Ensures efficient and effective day-to-day operations of the CE laboratory. This position reports ... Bachelor's Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with ...
Ensures efficient and effective day-to-day operations of the CE laboratory. This position reports ... Bachelor's Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with ...
Ensures efficient and effective day-to-day operations of the CE laboratory. This position reports ... Bachelor's Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with ...
Ensures efficient and effective day-to-day operations of the CE laboratory. This position reports ... Bachelor's Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with ...
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 ...
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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 ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
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 ...
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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 ...
cGMP Quality Control (QC) Specialist
Los Angeles, CA · On-site
$87K - $92K/yr
The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
Los Angeles, CA · On-site
$87K - $92K/yr
The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
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 ...
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 ...
QC, Analyst I
$24.50 - $33/hr
Legend Biotech is seeking a QC Analyst I (IPL) as part of the Quality Operations team based in Raritan, NJ . Role Overview The QC Analyst (IPL) is an exempt level position with responsibilities for ...
QC, Analyst I
$24.50 - $33/hr
Legend Biotech is seeking a QC Analyst I (IPL) as part of the Quality Operations team based in Raritan, NJ . Role Overview The QC Analyst (IPL) is an exempt level position with responsibilities for ...
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 ...
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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 ...
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 ...
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 ...
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 ...
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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 ...
Senior Scientist, Quality CMC
Portage, IN · On-site
Minimum of 8 years in pharmaceutical/biotech Quality Control, Chemistry, Manufacturing Controls (CMC), or Analytical Sciences * Demonstrated ownership of complex OOS, OOT, and deviation ...
Senior Scientist, Quality CMC
Portage, IN · On-site
Minimum of 8 years in pharmaceutical/biotech Quality Control, Chemistry, Manufacturing Controls (CMC), or Analytical Sciences * Demonstrated ownership of complex OOS, OOT, and deviation ...
Quality Control Technician
Alpharetta, GA · On-site
$20 - $24.57/hr
Keep up-to-date on QC related topics and share information with colleagues. • Suggest possible ... Qualifications • Bachelor Biomedical, Biotechnology, Laboratory • Experience with relevant ...
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Quality Control Technician
Alpharetta, GA · On-site
$20 - $24.57/hr
Keep up-to-date on QC related topics and share information with colleagues. • Suggest possible ... Qualifications • Bachelor Biomedical, Biotechnology, Laboratory • Experience with relevant ...
Quality Control Technician
Alpharetta, GA · On-site
$20 - $24.57/hr
Keep up-to-date on QC related topics and share information with colleagues. • Suggest possible ... Qualifications • Bachelor Biomedical, Biotechnology, Laboratory • Experience with relevant ...
Quality Control Technician
Alpharetta, GA · On-site
$20 - $24.57/hr
Keep up-to-date on QC related topics and share information with colleagues. • Suggest possible ... Qualifications • Bachelor Biomedical, Biotechnology, Laboratory • Experience with relevant ...
QC Inspector
Bothell, WA · On-site
$41K - $66K/yr
At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...
QC Inspector
Bothell, WA · On-site
$41K - $66K/yr
At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...
QC Inspector
$41K - $66K/yr
At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Minimum Education: Bachelor's degree in a related field strongly ...
QC Inspector
$41K - $66K/yr
At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Minimum Education: Bachelor's degree in a related field strongly ...
The organization is an Indianapolis based biotechnology company seeking applicants for a position in its Quality Control department. Education/experience * The appropriate candidate will have an ...
Quick apply
The organization is an Indianapolis based biotechnology company seeking applicants for a position in its Quality Control department. Education/experience * The appropriate candidate will have an ...
QC Inspector
$41K - $66K/yr
At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...
QC Inspector
$41K - $66K/yr
At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...
Day Biotech Quality Control information
See salary details
$12.98 - $14.51
1% of jobs
$14.51 - $16.04
6% of jobs
$16.04 - $17.57
12% of jobs
$18.06 is the 25th percentile. Wages below this are outliers.
$17.57 - $19.10
18% of jobs
The median wage is $20.12 / hr.
$19.10 - $20.63
19% of jobs
$20.63 - $22.16
15% of jobs
$22.75 is the 75th percentile. Wages above this are outliers.
$22.16 - $23.69
10% of jobs
$23.69 - $25.22
9% of jobs
$25.22 - $26.75
4% of jobs
$26.75 - $28.28
3% of jobs
$28.28 - $29.81
3% of jobs
$12
$20
$29
How much do day biotech quality control jobs pay per hour?
What is the difference between Day Biotech Quality Control vs Day Biotech Quality Assurance?
| Aspect | Day Biotech Quality Control | Day Biotech Quality Assurance |
|---|---|---|
| Primary Focus | Testing and inspecting products to ensure quality standards are met | |
| Responsibilities | Conducting lab tests, analyzing samples, documenting results | |
| Work Environment | Laboratories, manufacturing facilities | |
| Certifications | Relevant 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.
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 3 days ago
Job description
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.
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