Total 310 research associate job vacancies in Manufacturing / Production category in The United States of America

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

     

JOB DESCRIPTION:

Job Title

Associate Product Quality Analyst

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Burlington, MA location in the Heart Failure Division. In Abbott’s Heart Failure (HF) business, we’re developing solutions to diagnose, monitor and manage heart failure, allowing people to restore their health and get on with their lives.

This person analyzes customer complaints to determine which are regulatory reportable and coordinates activities with internal, field, and end use customers. They are responsible for adherence to Good Manufacturing Practices (GMPs) and proper complaint handling per the Code of Federal Register (CFR) and other governmental regulations. They will communicate event investigation results via regulatory reports and written communications, as appropriate.

What You’ll Work On:

• Review complaint communications and assess for regulatory compliance, reportability, and potential impact to patient safety and business operations.
• Participate in development and modification of these decision models with changes in product advances/therapies to uphold consistent compliance with government-mandated regulations.
• Evaluate and investigate identified complaints by gathering sufficient data from clinical staff, field representatives, internal employees, and laboratory analysis.
• Collect, compile, and document regulatory reportability decisions using event investigation and regulatory decision models.
• Draft Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring timely transmission to the appropriate regulatory authorities.
• Apply codes to events to facilitate product performance records.
• Review coding and investigations with engineering, laboratory, and other internal staff.
• Draft written communications detailing the clinical observation, investigation and/or product analysis, and corrective actions, as applicable, to physician and other end use customers.
• Communications include determination/eligibility for warranty credit or unreimbursed medical payments.
• Begin establishing and cultivating a network of internal resources to facilitate completion of tasks.
• Individual influence is typically exerted at the peer level.
• Completes daily work to meet established schedule with guidance from supervisor on prioritization of tasks.
• May exercise authority within pre-established limits and approval.
• Failure to achieve results can normally be overcome without serious effect on the business.

Required Qualifications

• Bachelor’s Degree (± 16 years) or Related field an equivalent co
• 0-2 years of related work experience with a basic understanding of specified functional area.

Preferred Qualifications

• General knowledge and basic application of business concepts, procedures and practices.
• Will perform this job in a quality system environment.
• Failure to adequately perform tasks can result in noncompliance with governmental regulations.
• Learns to use professional concepts and company policies and procedures to solve routine problems.
• Works on problems of limited scope.
• Minimal independent decision making.

* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.

     

The base pay for this position is

$48,000.00 – $96,000.00

In specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Operations Quality

     

DIVISION:

HF Heart Failure

        

LOCATION:

United States > Massachusetts > Burlington : 168 Middlesex Turnpike

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

No

     

MEDICAL SURVEILLANCE:

No

     

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)

     

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

     

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

     

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

The Asahi Kasei Group operates with a commitment of creating for tomorrow.  Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those around the world. We look for candidates that offer a fresh perspective and a variety of skills to help us achieve our commitment.

Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients’ expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team. Bionova became a subsidiary of Asahi Kasei Medical in May 2022, a division of Tokyo-based Asahi Kasei Group. This acquisition has enabled Bionova to greatly accelerate growth of the business, both in capacity of current service offerings and expansion into new service offerings.

Company:

Bionova Scientific LLC

Job Description:

Company Summary:

Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems.

Because our success depends on our ability to exceed our clients’ expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team.

Position Summary:

The Senior Manufacturing Associate will actively contribute to the manufacturing projects at the Bionova Scientific West Warren site.  As part of the Aseptic Operations Manufacturing group, you will have opportunities to work on and take ownership of a wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, facility buildout, and tech transfers of processes into a GMP multi-product manufacturing facility.  The role will provide hands-on execution of complex experiments in a team setting. The role will support GMP readiness and manufacturing activities.  The scope of responsibilities may include but are not limited to Document writing (SOPs, Equipment URSs, etc.), equipment validation execution support and single-use assembly design.

Essential Duties and Responsibilities:

• Executes complex unit operations including but not limited to cell culture thaw, expansion, generation and maintenance of Master and Working Cell Banks, End of production banking, and drug product filling.
• Performs internal support activities such as maintenance of analytical and product filling equipment, stocking of consumables, discarding expired reagents, material coordination and weigh and dispense.
• Maintains own training within compliance and trains other GMP associates upon completion of trainer qualification.
• Support in equipment troubleshooting, pilot scale material generation, non-GMP tox material generation and GMP Upstream, GMP Dowstream, and Bulk Fill activities.
• Author/review/approve technical documents such as tech transfer protocols and reports, experimental plans, production batch records, training materials, manufacturing SOPs, and regulatory filing documents per project needs.
• Documents work according to cGMP and cGDP.
• Adheres to established regulations and follows cGMP established by site. 
• Maintain cleanroom standards, practices, and housekeeping according to SOPs. 
• Recognize any minor issues from the equipment and any affiliated documentation and take appropriate corrective action within scope.  Notify leads/managers of issues and discrepancies immediately.   
• Assess impact of issues and non-conformities to products and projects as they pertain to product safety and efficacy or project milestones. 
• Evaluate new technologies and innovations to improve operational efficiency or expand cell culture capabilities.
• Contributes to quality activities such as investigations and area walk-throughs and support authoring deviations, CAPA, change control. 
• MSAT support, Material receipt, and inventory organization.
• Other duties as assigned to ensure appropriate compounding practices

Working Conditions:

• This position is required to work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching.  The employee must occasionally lift and or move up to 20 pounds independently.

Qualifications

• BS in Engineering, Life Sciences, or related discipline with 2+ years of relevant experience; AA degree with combination of industry experience and relevant degree; or combination of experience and relevant advanced degree, preferably in biopharma manufacturing role. 
• Must have aseptic technique experience.
• Basic Upstream and/or Downstream experience is a plus
• Cell Banking experience is a plus.
• Working knowledge of cGMP compliance as it pertains to procedures, processes, and manufacturing
• Creative thinker that can identify better and more efficient methods to address issues and gaps.
• Demonstrate ability to work independently and on cross-functional teams.
• Ability to handle more than one task at a time, while maintaining attention to detail and working in a fast-paced environment.
• Strong analytical skills and attention to detail.
• Flexible mindset for a dynamic environment.
• Flexibility with work hours to meet business needs, including weekends and holidays, as needed.

Compensation Range: The base compensation range for this role is between $32-40 an hour. However, the actual compensation may vary depending on your experience and qualifications.

Bionova offered Benefits and Program

Healthcare, Dental, and Vision insurance: Bionova offers health benefits at a subsidized rate.

Life Insurance and Disability Program: Life insurance is offered at 2x of annual base pay. Life insurance benefits start from the first day of employment. Disability programs are 100% covered by Bionova; a waiting period may apply as per company policy. 

Retirement Plan (401K) up to 8% employer match: 3% safe harbor contribution towards an employee's retirement plan and matches up to 5% dollar-for-dollar of base pay.

Paid time off

Holiday:

As an equal opportunity employer, Asahi Kasei believes a diverse workforce will provide us with the ability to continuously support the changes in the economy, society, and environment.

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.

We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a MS&T PRODUCT STEWARD, supporting our MANUFACTURING SCIENCE & TECHNOLOGY TEAM , you will be trusted with owning the process knowledge of the products assigned throughout the commercial lifecycle, maintaining oversight on process capability, through data trending and statistical analysis of critical parameters, ensuring processes are robust, in continued state of validation and continuously improving and in compliance with cGMPs, SOPs, and applicable guidelines and normatives at the ASPEX FORT WORTH MANUFACTURING FACILITY in FORT WORTH, TEXAS, US.  

In this role, a typical day will include:

• Process/Product Oversight and Knowledge: Maintain the oversight of the process of the product(s) assigned “door to door” at the site.

• Maintain the knowledge and the history of the product(s) process throughout the entire commercial lifecycle, from inception to date.

• Primary contact with R&D as the plant Sustaining Scientist.

• Oversee implementation of systems, policies and procedures to ensure that products and services meet regulatory and quality standards.

• Monitor processes, identify problems and initiate appropriate corrective actions, including deployment of available resources.

• Monitor, analyze and recommend/implement improvements to better utilize labor, raw materials and equipment.

• Manage significant projects.

• Determine and communicate priorities and schedules between potentially conflicting areas.

• Monitor, analyze, and control variables.

• Maintain awareness of state-of-the-art equipment and processes; recommend and implement changes, as applicable.

• Prepare analyses and provide input to Site Management for use in strategy setting.

• Critically review operations for ways to improve regulatory compliance, aseptic techniques, product quality and/or productivity.

• Track, evaluate and report on key indicators, as well as corrective and preventive actions.

• Investigations/Improvement on Product: Initiate and support investigations and improvement projects involving cross functional teams based on data analysis.

• Actively participate and represent assigned products to the relevant governance where improvements on weak point products are planned, prioritized and monitored.

• Provide oversight and support of the Continued Process Verification (CPV) program.

• Change Control: Participate and/or lead (case by case) the change control of assigned products and related processes.

• APQR: Review the PQR data and provide the correct level of discussion on it.

• Training: Own the Training Curriculum for assigned Job Profile and provide training and support to new associates joining related functions.

• Audit Support: Maintain assigned documentation and work area in inspection readiness level and provide necessary support in any internal or external audit.

• Provide a safe working environment that complies with applicable standards, and that associates are working safely.

• Continuously monitor work areas; identify, resolve, and report safety hazards.

WHAT YOU'LL BRING TO ALCON:

• Bachelor’s Degree or Equivalent years of directly related experience (or high school +13 yrs; Assoc.+9 yrs; M.S.+2 yrs; PhD+0yrs)

• The ability to fluently read, write, understand and communicate in English

• 5 Years of Relevant Experience

• Work hours: Monday through Friday – 8:00am – 5:00pm

• Travel Requirements: 0 to 10%

• Relocation assistance: No

• Sponsorship available: No

PREFERRED QUALIFICATIONS:

• Bachelor’s Degree in Pharmacy, Pharmaceutical Technology, Chemistry or equivalent scientific or engineering degree

• 6 or more years of relevant experience in pharmaceutical manufacturing

• Proven process understanding of Pharma, GMP, Regulatory aspects

HOW YOU CAN THRIVE AT ALCON:

• Collaborate with teammates to share standard processes and learnings as work evolve

• See your career like never before with focused growth and development opportunities

• Join Alcon’s mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!

• Alcon provides robust benefits package including health, life, retirement, flexible time off for exempt associates; PTO for hourly associates, and much more!

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

Find Jobs for Employees

Find Jobs for Contingent Worker

  

Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.

• Prepare, setup and qualify machines before shipping out from factory to customer.
• Support site service as to when required.

Requirements:

• Diploma in Mechatronics
• At least 2 years of working experience in mechanical/electrical control system.
• Good understanding of machinery automation with electrical, servo, sensor, pneumatic system.

If you are keen to apply for the position, kindly email your detailed resume in MS Word to hr@recruit-expert.com

Please note that only shortlisted candidates will be notified.

For more job opportunities, please visit our website at www.recruit-expert.com

EA Licence: 19C9701
Registration: R21100996

Tower Research Capital, a high-frequency proprietary trading firm founded in 1998, seeks a Production Trader to join one of its trading teams in Singapore. As a Production Trader, you will play a crucial role in day to day monitoring of all the automatons trading across all the Asian Markets.

Responsibilities

• Monitoring morning/evening maintenance operation
• Intraday monitoring of all the trading automatons: internal KPIs, Tower Risk Limits
• Ensuring intraday communication with the internal Compliance and Risk department
• Monitoring and Hedging some exposures manually
• Providing feedback and analysis to quants on algo behavior to help them improve models

Requirements

• Bachelor's degree in Computer Science, Engineering, or a related field. A Master's degree is preferred.
• At least 4 years of equivalent practical experience
• Good knowledge of Asian Derivatives and Cash Markets
• Strong problem-solving skills and the ability to work in a fast-paced, collaborative and geographically distributed environment
• Excellent communication and teamwork abilities
• Good knowledge of both Equities and Equity Derivatives trading
• Experience with scripting and programming languages such as Python and Bash

Nice to Have

• Experience with workflow management and task scheduling
• Experience in Index Arbitrage systematic trading
• Specific trading knowledge in any major Asian Exchanges

Evotec (US) Inc. is an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

Build a career powered by innovations that matter!  At Novanta, our innovations power technology products that are transforming healthcare and advanced manufacturing—improving productivity, enhancing people’s lives and redefining what’s possible.  We create for our global customers engineered components and sub-systems that deliver extreme precision and performance for a range of mission-critical applications—from minimally invasive surgery to robotics to 3D metal printing.

Novanta is one global team with over 26 offices located in The Americas, Europe and Asia-Pacific.  Looking for a great place to work?  You have found it with a culture that embraces teamwork, collaboration and empowerment.  Come explore Novanta.

Job Summary and Primary Responsibilities:

Market Research:

• Conduct primary and secondary market research with a focus on the medical diagnostic segments to identify trends, opportunities, and potential areas for product improvement and segment expansion.
• Supporting our Product Managers, collaborate with internal teams, including engineering, marketing, and sales, to define and prioritize market-driven product features and enhancements.
• Stay informed about industry trends, competitor products, and emerging technologies.

Portfolio Management:

• Assist Product Managers in the development of product roadmaps, ensuring alignment with JADAK objectives.
• Assist in the introduction of new products, working with the PMs to create business cases and product docs.
• Collaborate with sales and marketing teams to develop go-to-market strategies for product launches.
• Conduct pricing analysis to inform the price increase process.

Sales Enablement:

• Work closely with product management to support product launches and actively engage with the sales team to maximize revenue achievement.
• Leveraging analytical skills to analyze incoming mix deals and work with the commercial team to focus on the applications where we have the right to win.

Requirements:

• Experience in product management, engineering, market research, or a related role.
• Experience and strong passion in the medical devices industry a plus.
• Strong analytical and problem-solving skills. Advanced knowledge of Microsoft Excel required.
• Excellent communication and collaboration abilities

Education:

• Bachelor's degree in business, Analytics Marketing, Engineering, or a related field

Physical Requirements:

• Mobility to work in a standard office setting and to use standard office equipment, including a computer.
• Ability to use vison to read computer screen and read printed materials.
• Ability and willingness to travel 10-15%

Compensation and Benefits:

• The base pay for this position is $52,289 to $71,897 per year depending on the geographic market.
• Dependent on the position offered, annual bonuses and other forms of compensation may be provided as part of the compensation package.
• Novanta supports all aspects of your life’s needs.  This position provides a full range of medical, financial, and other benefits to make your quality of life better.

Novanta is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy.

Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process.

Every day, Global Payments makes it possible for millions of people to move money between buyers and sellers using our payments solutions for credit, debit, prepaid and merchant services.  Our worldwide team helps over 3 million companies, more than 1,300 financial institutions and over 600 million cardholders grow with confidence and achieve amazing results.  We are driven by our passion for success and we are proud to deliver best-in-class payment technology and software solutions.  Join our dynamic team and make your mark on the payments technology landscape of tomorrow. 

Position Overview

The Associate Product Manager will work with teams across the Global Payments organization in order to gain a deep understanding of the systems and platforms that power Unified Payments. They will work closely with our partners within each region in order to build a picture of their needs from both a Product and Sales perspective as well as their market demands and platform capabilities, both existing and new.

The ideal candidate for this role will have a strong technical ability and enjoy taking on complexity while at the same time having a strong strategic and commercial acumen to be able to see the “bigger picture”. Collaboration and coordination with multiple regions and business units is essential including Asia, Latin America, EMEA and North America.

This is an exciting role with potential for the right candidate to develop and grow a critical offering within the Global Payments Product organization.

Duties & Responsibilities

1. Deliver an excellent API integration and in-life processing experience to our customers across our global footprint 
2. Own and continuously seek to improve those products, standards, processes and working methods that are needed to execute API integrations and API in-life support. Seek out demand from the market and internal stakeholders, ideate solutions and prioritise change on these products and processes. 
3. Work closely with Support Engineer teams across Global Payments to govern API integrations and in-life support ensuring a high quality experience is maintained, supported by excellent product and processes. 
4. Ensure effective training and communication is in place for all teams supporting integrations and inlife support. Acquire information that affects API integration and support information and disseminate this information in a timely manner to appropriate teams. 
5. Ensure the Global Payments Developer Portal is up to date with the latest API information and features. 
6. Be a strong customer advocate, responding to and managing customer implementations and escalation. 
7. Be involved in strategic projects with a strong passion to deliver exceptional customer experience outcomes. 
8. Curious and able to think creatively, this person will analyse and deploy solutions to problems on the fly as well as implementing best practices to ensure that problems won’t recur. 
9. All other duties as assigned

Abilities & Behaviors

The ideal candidate will be able to demonstrate strong aptitude in the following areas:

• Problem solving and attention to detail

• Communication and presentation skills

• Analytical, interpretive and organizational abilities

• Relationship management and interpersonal skills

• Confident and decisive decision making

• Customer focussed and oriented

Qualifications & Experience

• A minimum of 2 years experience as an Associate Product Manager / Business Analyst or relevant experience in a digital business

• Payments industry experience is a plus

• A bachelor’s degree from college or university or comparable market experience or training

• Established technical aptitude, understanding of and working with commerce (or similar) ecosystems, platforms and tools

• Demonstrated communication skills with peers and senior stakeholders

• Self-motivated with a proven track record of delivering success while operating within a team environment

• Experience with business intelligence tools such as Tableau or Looker Studio is a plus

Global Payments Inc. is an equal opportunity employer.

Global Payments provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex (including pregnancy), national origin, ancestry, age, marital status, sexual orientation, gender identity or expression, disability, veteran status, genetic information or any other basis protected by law. Those applicants requiring reasonable accommodation to the application and/or interview process should notify a representative of the Human Resources Department.

     

JOB DESCRIPTION:

Function as a key person for application and technical supports of Abbott Rapid Diagnostics (ARDx) business in Thailand by supporting Abbott’s direct salesforce and distribution partners’. Responsible for post-sale supports to end users. This includes user training, preparing work instruction of products, troubleshooting, and technical complaints handling to ensure that the products perform at their best level.

Support sales activities through preparation of marketing materials including product sell sheets & specification and conducting technical sales pitches. Assist his/her line manager on KOL engagement and demand generation through CME/ CMTE/ CPE activities

·       Provide marketing, application support and technical assistance, troubleshooting and training to existing and potential users of ARDx products as well as distribution partners in Thailand

·       Manage incident and related quality assurance or handling of product complaints

·       Act as a liaison between Thailand ARDx and SEA Tech Support on reporting technical incidents of products and solve them on a timely manner

·       Visit and assist customers in properly understanding and utilising the products as well as provide updates on ARDx product range

·       Work with appointed distributors/ dealers to respond to technical enquiries of products

·       Assist his/ her line manager to develop and maintain cordial business relations with key opinion leaders and policy makers from various institutions

·       Assist in marketing and demand generation activities such as local events / congress when

Perform other tasks as assigned.

Qualification

·       Bachelor’s degree in Medical Technology, Biochemistry, or equivalent.

·       Minimum 3-year experience in the IVD sector with proven professional records as Product Specialist, Application Specialist, Techincal Supports, or equivalent. 

·       Professional experience in rapid dignostics or point-of-care testing is preferable 

·       Withhold knowledge of laboratory medicine, infectious dieseaes, clinical immunology, good laboratory practice, and quality management of clinical laboratory  

Fair command of English with good reading and writing competency

for candidate who interested in this position, please do think link https://assessment.predictiveindex.com/S5X/ab04e949-7a39-41b0-ad8f-35de671b947d?type=candidateba

     

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Product Management

     

DIVISION:

IDEM ARDx Infectious Disease Emerging Markets

        

LOCATION:

Thailand > Bangkok : Q-House Lumpini Building

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

Yes, 25 % of the Time

     

MEDICAL SURVEILLANCE:

Yes

     

SIGNIFICANT WORK ACTIVITIES:

Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)

     

     

     

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.

We foster an inclusive culture and are looking for diverse, talented people to join Alcon As a Production Technician supporting LS3, you will be trusted to deliver all aspects of production processes at our Manufacturing Facility in Johns Creek, GA.

In this role, a typical day will include:

• Perform minor equipment repairs and adjustments and conduct autonomous maintenance along with 5S duties.
• Coordinate downtime to ensure efficient use for maintenance and cleaning.
• Operate production equipment, perform lot changes, and coordinate machinery downtime.
• Troubleshoot equipment faults and enter product and raw materials into MES and SAP databases.
• Work with engineers to execute equipment validations.

WHAT YOU'LL BRING TO ALCON:

• High School Diploma or Equivalent.
• The ability to fluently read, write, understand, and communicate in English.
• Work hours: 6:30PM - 6:30AM; 12-hour rotating night shift: 2 nights on, 2 nights off, and every other weekend.
• Travel Requirements: None
• Relocation assistance: No
• Sponsorship available: No

HOW YOU CAN THRIVE AT ALCON:

• Join Alcon’s mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!
• Alcon provides robust benefits package including health, life, retirement, flexible time off, and much more!

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

Find Jobs for Employees

Find Jobs for Contingent Worker

  

Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.

• Prepare, setup and qualify machines before shipping out from factory to customer.
• Support site service as to when required.

Requirements:

• Diploma in Mechatronics
• At least 2 years of working experience in mechanical/electrical control system.
• Good understanding of machinery automation with electrical, servo, sensor, pneumatic system.

If you are keen to apply for the position, kindly email your detailed resume in MS Word to hr@recruit-expert.com

Please note that only shortlisted candidates will be notified.

For more job opportunities, please visit our website at www.recruit-expert.com

EA Licence: 19C9701
Registration: R21100996

Evotec (US) Inc. is an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

Career Category

Supply Chain

Job Description

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us as:

Production Planner (Senior Associate Supply Chain – Detailed Scheduler)

At Amgen, Breda medicines are labeled, assembled, stored, and shipped to various countries worldwide. Every day more than 1000 people from 38 different nationalities work on supply chain processes, manufacturing, marketing, and sales of our medicines and clinical research into new drugs.

Live

What you will do

Our Supply Planning team plays a key role in fulfilling Amgen’s mission. We ensure supply to patients in close to 100 markets in Europe, Turkey, the Middle East, and Africa Regions. As part of the operations team located in Breda, we are responsible for managing the short-, medium-- and long-term plans for incoming supplies for production and warehouse. The Amgen Breda site is Class A certified and widely recognized in the Amgen network for its capabilities to deal with high complexity, short lead times, and stable operation.

We are looking for a Detailed Scheduler to support our Supply Planning team: junior or experienced Supply Chain professional. Do you like new challenges? Then let’s do this. Let’s change the world.

In this role, you will:

• Manage short-term production planning for packaging lines, ensuring timely delivery and stable supply chains to our patients.
• Craft production plans, manage orders, drive timely delivery, and support phase-in-phase-out of products and launches.
• Measuring weekly and monthly KPI’s for the Master Production Schedule Stability and setting actions towards stakeholders for improvement.
• Participate and facilitate daily operational meetings to oversee performance and coordinate actions across departments.
• Collaborate closely with manufacturing, quality, warehouse, and supply chain; lead weekly capacity meetings to align on realistic supply plans.

• Drive standardization, simplification, and automation of processes in your daily work as well as in cross-functional projects.
• Lead continuous improvement initiatives and root cause analyses.
• Demonstrate leadership in ensuring stable operations and supply chain efficiency while adhering to and within GMP and GDP guidelines.

Win

What we expect of you

We are all different, yet we all use our outstanding contributions to serve patients. The supply chain and planning professional we seek is detailed oriented and a strong collaborator with these qualifications:

• Bachelor's or Master’s Degree in a business, supply chain, science, engineering, or related discipline.
• Experience with supply chain planning.
• Strong interpersonal and collaborative skills.
• Analytical skills to evaluate root cause analysis and problem-solving skills in a team environment.
• Experience in regulated Good Manufacturing Practice (GMP) is not required but will be beneficial.
• Passionate about standardization and process automation. Interest and/or experience with Tableau, Smartsheet, Databricks, RPA is preferred.
• To have enough connection with the shopfloor, this role will work hybrid with at least 3 days in the office on average.

Thrive

What you can expect of us

We work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being. Therefore, Amgen is regularly recognized as a Great Place To Work ©.

• Vast opportunities to learn and move up and across our global organization.
• A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act.
• Generous Total Rewards Plan comprising competitive salary, bonus structure, fixed 13th month, holiday allowance, and collective health insurance.
• Focus on vitality with an on-site gym, a vitality program, and a restaurant with healthy food.
• The flexibility of working from home and being in the office allows you to meet your new colleagues both virtually and face to face.

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ABOUT KATALON

Founded in 2016, Katalon is the leading provider of a modern, comprehensive quality management platform. Katalon Platform enables quality assurance, DevOps, and software teams of any size to deliver world-class customer experiences faster, easier, and more efficiently.

Since its first launch, Katalon has experienced tremendous growth, serving more than 100,000 users across 30,000 teams of all shapes & sizes, many of which are in the Fortune Global 500, such as PwC, KMPG, Abbott, Standard Chartered, etc. Katalon is recognized as a top automation tool by prestigious review sites, such as Gartner, Capterra, and IT Central Station.

Katalon is headquartered in Atlanta, GA. For more info about Katalon, please visit https://katalon.com/

ABOUT POSITION

Calling all passionate Associate Product Managers! If you thrive in fast-paced environments and are eager to collaborate with both product and engineering teams to drive innovation, then this role is for you.

Here's a snapshot of what you'll be doing:

• Insightful Requirement Gathering: Delve deep into user needs and market trends to craft high-level requirements.
• Creative Prototyping and Design: Actively contribute to agile prototyping processes, shaping intuitive interfaces and wireframes.
• Market Analysis and Competitive Intelligence: Stay ahead of the curve by analyzing market trends and competitor moves.
• Empowering Development Teams: Translate business vision into actionable insights for development squads.
• Strategic Roadmap Definition: Collaborate with Product Managers to define clear product visions and roadmaps.
• Feature Prioritization and Release Management: Strategically prioritize features and manage release cycles effectively.
• Cross-Functional Coordination: Bridge gaps between teams to ensure cohesive product launches and ongoing success.
• Idea Cultivation and Promotion: Foster innovation by identifying and promoting promising ideas.
• Feedback Integration and Iterative Improvement: Seamlessly integrate user feedback into our development processes for continuous improvement.

If you're ready to make an impact and drive transformative change, we want to hear from you! Join us and be part of a team that's shaping the future of our products every day.

Key Qualifications:

• Practical Experience: Bring at least 2 years of hands-on experience from roles like Product Owner or IT Business Analyst, showing us your ability to roll up your sleeves and get things done.
• Agile Proficiency: Proficient in Agile and Scrum methodologies, with a track record of applying these practices effectively in product development.
• Stakeholder Management: Demonstrated ability in stakeholder management and delivering compelling presentations that engage and align stakeholders.
• Language and Tech Skills: Advanced proficiency in English coupled with a keen aptitude for learning and adapting to new and emerging technologies.
• Requirement Specification: Familiarity with requirement specification techniques including user story development, modeling, and prototyping.
• Analytical Abilities: Strong organizational and analytical skills, coupled with excellent oral and written communication abilities.

Nice to Have:

• Automation Testing Experience: Experience in Automation Testing is highly desirable and considered a significant advantage.
• Educational Background: Bachelor's Degree in Computer Science or a related technical discipline is preferred, although equivalent practical experience will also be considered.
• Software Industry Domain Expertise: Previous exposure to the software industry, particularly in SaaS, and an understanding of complex technical challenges will be beneficial.

At Katalon, we bring together self-starting, open-minded, and talented people while actively promoting a transparent and growth-enabling working environment. But don’t just take our word for it. Take a better look below!

• Attractive compensation package: Embrace periodic performance and 13th-month bonuses;
• Generous time-off: Enjoy 19 annual leave days, supportive allowances, and public holidays;
• Flexible work arrangements: Tailor your work to your needs by applying our hybrid working policy together with high-end working equipment;
• Vibrant international workspace: Fostering an Agile Culture at Viettel Building, D.10, HCMC;
• Premium healthcare coverage: For both you and your loved ones;
• Exciting company events: Embark on summer trips, annual parties, team-building activities, and so much more fun are waiting for you.!

Katalon is proud to be an equal-opportunity employer. We care about our people and celebrate our differences. We want to work with talented, collaborative, and innovative people. We do not discriminate in hiring or any employment decision based on race, color, religion, national origin, age, sex (including pregnancy, childbirth, or related medical conditions), marital status, ancestry, physical or mental disability, genetic information, veteran status, gender identity or expression, sexual orientation, or other characteristics protected by law.

Career Category

Operations

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Associate Manufacturing - Night Shift-D

Live

What you will do

Let’s do this! Let’s change the world! In this vital role you will perform operations within the Manufacturing area, specifically solutions, at Amgen's innovative Rhode Island facility. You will be required to know, comprehend, and apply Good Manufacturing Practices (GMP), as well as understand, follow, and document in batch records.

• Perform batching and transfer of Buffers and Media in appropriate areas according to Standard Operating Procedures (SOPs).
• Follow and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports.
• Conduct basic troubleshooting and assist in the review of documentation for assigned functions.
• May also have the responsibility of initiating and owning area Deviations, revising SOP's and performing LEAN functions.
• Identify, recommend, and implement improvements related to routine functions.

In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (D- Shift). This includes extra benefits such as receiving an added 15% shift differential, and also getting premium pay for any Sundays worked. The schedule during the initial on-boarding/training phase (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an experienced individual with these qualifications.

Basic Qualifications:

• High school/GED + 2 years of manufacturing or operations work experience OR
• Associate’s + 6 months of manufacturing or operations work experience OR
• Bachelor’s Degree in a related field

Preferred Qualifications:

•  Bachelor’s degree in Science or Engineering
• Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc.
• Knowledge of Single-use-Systems
• CFR and Regulatory knowledge
• Mechanical ability/expertise
• Basic statistical mathematical skills
• Ability to interpret and apply GMP knowledge
• Understanding of analytical methods for manufacturing area
• Demonstrated technical writing capability
• Able to demonstrate project management skills and presentation skills
• Ability to understand, apply and evaluate basic chemistry, biology and physical principles
• Basic troubleshooting skills on production equipment
• Experience with Delta V
• Experience with lab equipment/testing

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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Salary Range

67,083.00 USD - 84,094.00 USD