Quality Control Associate Job at Solomon Page (Piscataway)

Quality Control Associate

This is a Finance position responsible for monitoring the quality of perishable ...

Location

United States , Hartford

Salary:

23.00 USD / Hour

Sysco

Expiration Date

Until further notice

Requirements

High school diploma or general education degree (GED)
Prior warehouse, inventory control or merchandising experience
Proficient in Microsoft Office
Effective written/oral communication skills
Strong analytical skills

Job Responsibility

Provide technical, customer relations, and personnel management for major programs and projects
Check produce in slots on a daily basis to make a certain product that is set up for shipping is up to acceptable standards
Communicate regularly with necessary parties on the company’s status on product quality
Communicate with Inventory Control Manager or Compliance Manager and buyers all quality issues and assists them in resolving them to ensure the customer receives the highest quality products possible
Monitor variance reports for accurate accounting of spoilage, warehouse damage, truck damage, etc.
Inspect inbound freight, warehoused product, and/or outbound product and document product condition
Analyze, identify, and propose action to the solution of problems associated with Quality Assurance
Observe all safety rules, regulations, and sanitation policies

Fulltime

Associate Quality Control (Microbiology)

Amgen is one of the world’s leading independent biotechnology companies. For ove...

Location

Singapore , Singapore

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Microbiology, Biological Sciences, Life Sciences or related technological field and 2 years of directly related experience
Associate’s Degree in Microbiology, Biological Sciences, Life Sciences or related technological field and 4 years of directly related experience
Diploma in Microbiology, Biological Sciences, Life Sciences or related technological field / GED and 6 years of directly related experience
At least 1-3 years of relevant professional work experience within the biopharmaceutical industry and QC laboratory experience preferred
Possess sound knowledge and understanding of GMP pharmaceutical operations and associated QC testing methods, inclusive of GMP laboratory operation
Experience with Quality Control testing and laboratory operations for common microbial testing methods and equipment (e.g. including but not limited to bioburden, endotoxin, microbial identification, environmental monitoring, microbial limits, growth promotion, biological indicators)
Able to interact effectively with variety of communication and working styles and ability to work well in teams
Ability to manage multiple simultaneous activities in a rapidly changing environment
Possess problem solving skills with the ability to apply logic and assess data to troubleshoot and reach decisions or solutions related to assay
Your selection for this role will be subject to fulfilling the medical requirements of this job scope

Job Responsibility

Execute testing and/or review for routine environmental, water, raw material and product testing (e.g. bioburden, endotoxin, qPCR, microbial ID etc.)
media, reagent and culture qualification (e.g. growth promotion, DNA positive controls, microorganisms culture types etc.)
Sample management such as sample logging, movement, storage of samples, reconciliation of sample receipt, aliquoting samples, management of stability samples, and sample shipment to Amgen network sites and/or contract labs
Involvement in document revisions and report writing
Involvement in method transfers, method validation/verification and sample type qualification
Laboratory housekeeping and document archival
Project management / Involvement in QC projects (e.g. Continuous Improvement/ Operational Excellence)
When required, able to support 12-hour rotating day shift (8am - 8pm), inclusive of weekends and public holidays

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Associate Quality Control (Microbiology)

Associate Quality Control (Microbiology) Amgen Singapore Manufacturing HOW MIG...

Location

Singapore , Singapore

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Microbiology, Biological Sciences, Life Sciences or related technological field and 2 years of directly related experience
Associate’s Degree in Microbiology, Biological Sciences, Life Sciences or related technological field and 4 years of directly related experience
Diploma in Microbiology, Biological Sciences, Life Sciences or related technological field / GED and 6 years of directly related experience
Have at least 1-3 years of relevant professional work experience within the biopharmaceutical industry and QC laboratory experience preferred
Possess sound knowledge and understanding of GMP pharmaceutical operations and associated QC testing methods, inclusive of GMP laboratory operation
Experience with Quality Control testing and laboratory operations for common microbial testing methods and equipment (e.g. including but not limited to bioburden, endotoxin, microbial identification, environmental monitoring, microbial limits, growth promotion, biological indicators)
Able to interact effectively with variety of communication and working styles and ability to work well in teams
Ability to manage multiple simultaneous activities in a rapidly changing environment
Possess problem solving skills with the ability to apply logic and assess data to troubleshoot and reach decisions or solutions related to assay

Job Responsibility

Execute testing and/or review for routine environmental, water, raw material and product testing (e.g. bioburden, endotoxin, qPCR, microbial ID etc.)
media, reagent and culture qualification (e.g. growth promotion, DNA positive controls, microorganisms culture types etc.)
Sample management such as sample logging, movement, storage of samples, reconciliation of sample receipt, aliquoting samples, management of stability samples, and sample shipment to Amgen network sites and/or contract labs
Involvement in document revisions and report writing
Involvement in method transfers, method validation/verification and sample type qualification
Laboratory housekeeping and document archival
Project management / Involvement in QC projects (e.g. Continuous Improvement/ Operational Excellence)
When required, able to support 12-hour rotating day shift (8am - 8pm), inclusive of weekends and public holidays
All listed tasks and responsibilities are deemed as essential functions to this position
however, business conditions may require reasonable accommodation for additional tasks and responsibilities

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Associate Quality Control Microbiology

In this vital role, you will be responsible for analytical testing, sample and d...

Location

United States of America , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

High school / GED + 2 years of quality control work experience
Associate's + 6 months of quality control work experience
Bachelor's degree
Degree in Microbiology with +2 years of quality control experience
GMP laboratory experience in the Pharmaceutical or Biotech industry
Availability to the third shift including rotative weekdays and weekends
Knowledge of regulatory compliance, safety protocols, and GMP standards
Strong attention to detail, with solid organizational and time management skills
Bilingual in Spanish and English
effective in technical writing and communication

Job Responsibility

Perform routine and non-routine laboratory procedures, including aseptic aliquoting and analysis for both compendial and non-compendial methods
Conduct or support activities such as sample testing, standards and reagent preparation, environmental monitoring, sample management, and equipment maintenance
Ensure accurate, complete, and timely documentation of laboratory work, and participate in document revisions as needed
Review, analyze, and communicate test results
may participate in investigations, audits, or approve laboratory results as applicable
Complete all work in compliance with established procedures and scientific/technical standards

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
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 an annual site shutdown
Flexible work models where possible

Fulltime

Associate Quality Control (Analytical)

Amgen is one of the world's leading independent biotechnology companies. For ove...

Location

Singapore , Singapore

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Chemistry, Biochemistry, Life Science or related technological field and 2 years of directly related experience OR Associate's Degree in Chemistry, Biochemistry, Life Science or related technological field and 4 years of directly related experience OR High School Diploma in Chemistry, Biochemistry, Life Science or related technological field / GED and 6 years of directly related experience
1-2 years of relevant laboratory experience in the commercial manufacturing environment within the pharmaceutical or biopharmaceutical industry and analytical testing experience preferred
Knowledge and understanding of GMP pharmaceutical production, pharmaceutical plant operation and associated testing methods
Experience with Quality Control testing and laboratory operations for common testing methods and equipment (e.g. including but not limited to UPLC, HPLC, LC-MS, GC-HS, LOD, Auto-titration, KF, Optical Rotation, wet chemistry, FT-IR, pH, conductivity, TOC, Potency, ELISA, Capillary Electrophoresis, DNA Testing)
Good communication skills (technical writing and verbal communication/ presentation)
Interact effectively with variety of communication and working styles and ability to work well in teams
Ability to manage multiple simultaneous activities in a rapidly changing environment
Problem solving skills and troubleshooting skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality.

Job Responsibility

Perform analytical testing of in-process control, drug substance intermediate, final release, stability and plant cleaning samples in a GMP pharmaceutical environment
Support laboratory operations including but not limited to equipment qualification, calibration, cleaning and maintenance, reagent/ buffer preparation
Responsible for maintenance of chemicals and consumables inventory
Ensure proper handling, storage, disposal of all chemicals used in the lab
Responsible for laboratory housekeeping and document archival duties
Participate in laboratory investigations and assist in timely closure of investigations, CAPAs and deviations
Participate in method verification and method validation/ transfer for new product introduction (when required)
Perform review of laboratory data/ records
Assist in SOP/ protocol/ report writing
Assist in periodic review of laboratory procedures and risk assessment

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Associate Quality Control

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States , Thousand Oaks

Salary:

62571.90 - 84656.10 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 2 years of Quality experience OR Associate’s + 6 months of Quality experience OR Bachelor’s

Job Responsibility

Responsible for one or more of the following activities in QC: analytical testing, sample and data management and equipment maintenance
Perform routine laboratory procedures such as sample analysis, standard and solution preparation
Responsible for documenting, compiling, interpreting, reviewing and entering laboratory data
Providing and communicating results, maintaining/operating specialized equipment and drafting and revising documents such as Analytical Methods, SOPs and technical reports
Support introduction of new methods/techniques into the lab
Perform basic assay and instrument troubleshooting

What we offer

A 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
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

Associate Quality Control

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States , Holly Springs

Salary:

76773.00 - 79317.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree (or foreign equivalent) in Microbiology, Biology, Biochemistry, or related field & completion of a university-level course, research project, internship, thesis, or one year of experience involving the following: Quality control testing including: Bioburden, Endotoxin and Microbial Identification
Environmental Monitoring, utilities sampling, and knowledge of EM and utilities programs
Participating in or leading Deviations, CAPAs or investigations
Maintaining laboratory equipment, including coordination of maintenance and calibration programs
Supporting review or authorship of standard operating procedures, safety assessments, and technical reports
cGMP and GLP work environment and best practices.

Job Responsibility

Assist execution of equipment installation and qualification within the microbiology lab to support start-up
Support document review and authoring, including: standard operating procedures, safety assessments, methods, trend reports, microorganism assessments, and technical reports
Assist with execution of Environmental Monitoring Performance Qualification activities to support establishment of environmental monitoring program
Perform routine environmental monitoring and utilities sampling
Perform routine quality control testing, including Bioburden, Endotoxin, Microbial Identification, Polymerase chain reactions, and total organic carbon
Participate in audits, initiatives, and projects that may be interdepartmental or global in scope
Participate in deviations, CAPAs, and cross functional investigations
Assist with general lab setup and 5S.

What we offer

stock
retirement
medical insurance
life insurance
disability insurance
eligibility for an annual bonus
health and welfare plans for staff and eligible dependents
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities

Fulltime

Senior Associate Quality Control I (Chemistry)

Amgen is one of the world’s leading independent biotechnology companies. For ove...

Location

Singapore , Tuas

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree in Chemistry, Biochemistry or related technological field
Bachelor’s degree in Chemistry, Biochemistry or related technological field and 2 years of directly related experience
Associate’s degree in Chemistry, Biochemistry or related technological field and/or 4 years of directly related experience
High school diploma in Chemistry, Biochemistry or related technological field / GED and 6 years of directly related experience
Preferred 4 years of relevant professional work experience within the pharmaceutical or biopharmaceutical industry and laboratory testing experience preferred
Strong knowledge and understanding of GMP pharmaceutical production, pharmaceutical plant operation and associated testing methods
Strong technical knowledge in and experience with the following QC Chemistry/ Biochemistry/ Raw material testing methods and equipment is required: Immunosorbent Assay/Cell based Bioassay: Potency, Host Cell Proteins, ELISA
Chromatography: UPLC, HPLC, LC-MS, GC-HS
General Chemistry: Capillary Electrophosis, LOD, Autotitration, KF, Optical Rotation, FT-IR, Conductivity, TOC, pH, wet chemistry
Ability to preempt issues and disruptions to lab operations and develop mitigation actions

Job Responsibility

Plan, schedule, perform analytical testing and approval of test results on raw materials, water, in-process control, drug substance and stability samples in GMP pharmaceutical environment
Troubleshooting issues related to analytical testing, techniques and equipment
Conduct laboratory investigations and assist in timely closure of investigations, CAPAs and deviations
Support method verification and method validation/transfer for new product introduction (when required)
Train new/ junior laboratory staff and ensure all staff are appropriately trained and qualified to execute the duties assigned to them with respect to the job
Support laboratory operations including but not limited to equipment qualification, calibration and maintenance, reagent/buffer preparation, chemicals/consumables inventory, laboratory housekeeping and document archival duties
Perform periodic review of laboratory procedures and risk assessment
Author of SOPs/protocols/reports
Support regulatory inspections
Participate in continuous improvement initiatives and projects

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

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Quality Control Associate

Job Description

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Requirements

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