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Day Biotech Quality Control Jobs (NOW HIRING)

TekWissen LLC

Quality Control Specialist

Vacaville, CA · On-site

$20 - $26/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Specialist II Location: Vacaville, CA, 95688 Duration: 6 Months Job Type: Temporary ...

Tunnell Consulting

Quality Control Manager

Raleigh, NC · On-site

... biotech, pharma, the U.S. Government, foundations, public/private partnerships, investors, and ... Our client is seeking a Quality Control (QC) Manager to lead both Microbiology and Analytical ...

Genentech

Quality Control Associate II

Oceanside, CA · On-site

$66K - $110K/yr

You possess a Bachelor's degree in Chemistry, Biochemistry, or a related scientific discipline with 5-6 years of experience in pharmaceutical/biotech QC labs, including hands-on raw material testing ...

New

TekWissen LLC

Quality Control Scientist

Vacaville, CA · On-site

$20 - $25/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate I / Quality Control Scientist Location: Vacaville, CA - 95688 Duration: 6 ...

BioLegend

Quality Control Supervisor

San Diego, CA · On-site

Oversee the day to day operations of the Flow QC group, including assigning testing samples to QC ... 6 years of biotech industry experience related to Quality Control * 2 years of experience ...

Legend Biotech US

Sr. QC Analyst

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech is seeking a Sr. QC Analyst as part of the Quality team based in Raritan, NJ . Role Overview The Sr. QC Analyst is an exempt level position with responsibilities for performing QC ...

Precigen, Inc

QC Manager

Germantown, MD · On-site

$95K - $120K/yr

... and biotech industry under GMP guidelines, with demonstrated expertise in multiple disciplines and assays. * 2+ years of supervisory experience. * Advanced experience with QC testing in ...

TekWissen LLC

Quality Control Analyst

Vacaville, CA · On-site

$20 - $25/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 ...

Peregrine Team

Quality Control Analyst

Seattle, WA · On-site

$27.25 - $36.75/hr

Peregrine Team is hiring a Quality Control Analyst to support laboratory testing and ensure product quality in a biotech environment. This role is essential to maintaining compliance and product ...

Pinnaql

Quality Control Manager

High Point, NC

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...

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How much do day biotech quality control jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for day biotech quality control in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What is the difference between Day Biotech Quality Control vs Day Biotech Quality Assurance?

AspectDay Biotech Quality ControlDay Biotech Quality Assurance
Primary FocusTesting and inspecting products to ensure quality standards are met
ResponsibilitiesConducting lab tests, analyzing samples, documenting results
Work EnvironmentLaboratories, manufacturing facilities
CertificationsRelevant lab certifications, GMP training

Day Biotech Quality Control professionals focus on testing products to verify quality, while Day Biotech Quality Assurance staff develop and maintain processes to prevent defects. Both roles are essential in biotech manufacturing, often working closely but with distinct responsibilities.

What cities are hiring for Day Biotech Quality Control jobs? Cities with the most Day Biotech Quality Control job openings:
What are the most commonly searched types of Biotech Quality Control jobs? The most popular types of Biotech Quality Control jobs are:
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Day Biotech Quality Control jobs near you
Manager, Quality Control Chemistry

Manager, Quality Control Chemistry

BeiGene, Inc.

Pennington, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
Manages all Quality Control (QC) Chemistry Laboratory - Capillary Electrophoresis (CE) activities to support GMP manufacturing, testing and release of materials, intermediates, and finished products under FDA/EU regulations, applicable International Regulations, BeOne processes and procedures. Establishes and implements QC Chemistry procedures including but not limited to capillary electrophoresis and supports regulatory compliance inspections. Ensures efficient and effective day-to-day operations of the CE laboratory. This position reports to the Senior Manager QC and is located full-time at the Hopewell, NJ site.
Essential Functions of the Job:
  • Lead the QC Chemistry (CE) laboratory daily workflow.
  • Establish and maintain QC Chemistry (CE) laboratory related quality systems to ensure conformance with regulations and BeOne Global quality standards.
  • Manage QC Chemistry (CE) laboratory routine operations, including but not limited to validation, SOPs, specifications, testing records, personnel training and assessment, scheduling, etc.
  • Ensure QC Chemistry (CE) laboratory compliance with Environmental Health and Safety (EHS) standards.
  • Ensure timely completion of testing (e.g., In-process control, DS release, DP release, and stability testing) to ensure timely generation and reporting of test results in support of manufacturing operations.
  • Review of laboratory test results, ensuring adherence to Good Documentation Practices.
  • Ensure appropriate investigation of OOS events, discrepancies, lab errors, and equipment failures.
  • Implementation of effective corrective actions and preventive actions (CAPAs).
  • Participate in internal and external GMP audits where possible.
  • Ensure that the QC Chemistry (CE) laboratory meets or improves on budget, cost, volume, and efficiency targets (KPIs) in line with business objectives.
  • Expertise in Quality Control (QC) within a Good Manufacturing Practice (GMP) environment, ensuring compliance with industry standards and regulations through hands-on laboratory experience.
  • Working knowledge and experience with capillary electrophoretic analytical methods such as reduced and non-reduced CGE, CZE, and cIEF/icIEF, etc.
  • Knowledgeable with USP/EP and cGMP/EU GMP regulations.
  • Familiar with instrument and equipment validation.
  • Expert knowledge of quality control principles, practices and standards for the biopharmaceutical industry.
  • Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level.
  • Strong leadership/team management skills and experience.
  • Manage, motivate, coach and mentor direct reports.
  • Credible and confident communicator (written and verbal) at all levels.
  • Strong analytical, problem-solving ability, with excellent attention to detail, with the ability to work accurately in a busy and demanding environment.
  • Excellent project management skills.
  • Hands-on approach, with a 'can do' attitude.
  • Ability to prioritize, demonstrating good time management skills.
  • Self-motivated, with the ability to work proactively using own initiative.
  • Committed to learning and development.
  • Interacts with all levels of BeOne employees
  • Undertake any other duties as required

Supervisory Responsibilities:
  • Manage direct reports from QC Chemistry (CE) laboratory
  • 2+ years of managerial experience directly managing people required
  • Leadership experience leading teams, projects, programs or directing the allocation of resources.

Computer Skills:
  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint).
  • Ability to work on a computer for extended periods of time

Travel:
  • Must be willing to travel approximately 10%

Education Required:
  • Bachelor's Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with 5+ years of GMP testing using capillary electrophoresis techniques in an FDA-regulated biotechnology, pharmaceutical company is required.
  • Bachelor's degree in Chemistry, Biology, Molecular Biology, Biotechnology, Biochemistry, or related scientific discipline preferred.
  • Master's degree and 4+ years of relative experience preferred.

Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $110,800.00 - $150,800.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media

Twitter

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