1

Contract Pharmaceutical Quality Control Jobs (NOW HIRING)

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) * Evaluate critical quality attributes (CQA) such as particle ...

Antheia is the advanced biosynthesis company transforming pharmaceutical manufacturing and ... Serve as the primary QC point of contact for CDMOs, CROs, and contract testing labs * Review and ...

Serve as the primary QC point of contact for CDMOs, CROs, and contract testing labs * Review and ... Advanced degree preferred. * 10+ years of progressive experience in pharmaceutical QC under GMP ...

$65K - $105K/yr

What You'll Do Analytical Testing & Expertise Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems) Evaluate critical ...

next page

Showing results 1-20

Contract Pharmaceutical Quality Control information

What are the key skills and qualifications needed to thrive as a Contract Pharmaceutical Quality Control specialist, and why are they important?

To thrive as a Contract Pharmaceutical Quality Control specialist, you need a strong background in chemistry, biology, or a related field, with experience in laboratory testing and quality assurance processes. Familiarity with analytical instruments such as HPLC, GC, and LIMS, as well as knowledge of regulatory standards like GMP and relevant certifications, is typically required. Attention to detail, problem-solving abilities, and strong communication skills are essential for accurate testing and effective collaboration. These skills and qualities ensure product safety, regulatory compliance, and the reliability of pharmaceutical products in a highly regulated industry.

What is the difference between Contract Pharmaceutical Quality Control vs Contract Pharmaceutical Quality Assurance?

AspectContract Pharmaceutical Quality ControlContract Pharmaceutical Quality Assurance
Primary FocusTesting and analyzing drug samples to ensure quality and complianceDeveloping, implementing, and maintaining quality systems and procedures
Work EnvironmentLaboratories, testing facilities, manufacturing sitesOffice settings, quality management departments, regulatory agencies
Required CredentialsDegree in pharmacy, chemistry, or related field; certifications in lab testingDegree in pharmacy, chemistry, or related field; certifications in quality systems
Industry UsageUsed by pharmaceutical companies during product testing phasesUsed for ensuring overall quality compliance and regulatory adherence

Contract Pharmaceutical Quality Control focuses on testing and analyzing pharmaceutical products to verify quality, while Contract Pharmaceutical Quality Assurance emphasizes establishing and maintaining quality systems to ensure compliance. Both roles are essential in the pharmaceutical industry but serve different functions within the quality management process.

What is Contract Pharmaceutical Quality Control?

Contract Pharmaceutical Quality Control refers to the process where pharmaceutical companies outsource the testing and analysis of their products to third-party laboratories or service providers. These contract labs ensure that drug products meet regulatory standards for safety, efficacy, and quality before they reach the market. Services often include analytical testing, microbiological testing, method development, and stability studies. By outsourcing this work, companies can access specialized expertise and equipment, streamline operations, and maintain compliance with global regulations.

What are some common challenges faced in a Contract Pharmaceutical Quality Control role and how can they be effectively managed?

In a Contract Pharmaceutical Quality Control role, professionals often navigate challenges such as tight project deadlines, varying client expectations, and strict regulatory requirements. Managing these challenges effectively involves clear communication with clients, thorough documentation, and staying updated with industry standards like GMP and FDA guidelines. Team collaboration is key, as projects typically involve coordination with analytical chemists, quality assurance specialists, and production staff. Adaptability and attention to detail are essential for ensuring both compliance and client satisfaction in a fast-paced, contract-based environment.
What cities are hiring for Contract Pharmaceutical Quality Control jobs? Cities with the most Contract Pharmaceutical Quality Control job openings:
What are the most commonly searched types of Pharmaceutical Quality Control jobs? The most popular types of Pharmaceutical Quality Control jobs are:
What states have the most Contract Pharmaceutical Quality Control jobs? States with the most job openings for Contract Pharmaceutical Quality Control jobs include:
Pharmaceutical Quality Control Manager

Pharmaceutical Quality Control Manager

Yoh, A Day & Zimmermann Company

Rosenberg, TX

$105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago


Job description

Yoh Life Sciences is hiring for a Pharmaceutical Quality Control Manager in Houston, TX.  The QC Manager will serve as a scientific liaison in the lab by supporting method development validation and verification of protocols in a regulated pharmaceutical laboratory environment. General responsibilities include analytical testing of raw materials, in-process samples, finished products and  laboratory instrumentation calibration, such as HPLC, GC, CE, ICP, FTIR, TOC, dissolution apparatus within a cGMP environment. This role requires a minimum of 8 years within a quality control or analytical chemistry laboratory.
Title: QC Manager
Duration: Permanent
Pay: $80,000-105,000 DOE
Location: Houston, TX
Shift: M-F 8-5pm
PRIMARY DUTIES AND RESPONSIBILITIES:
  • Write method validation protocols/reports and perform method development/validation/ verification for API and finished drug products. 
  • Familiar with analytical testing of raw materials, in-process samples, finished products, and analytical laboratory instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC, dissolution apparatus, etc.
  • Supervise the daily activities of the pharmaceutical QC laboratory by establishing testing priorities and schedules, and assignments of staff based on company priorities and objectives. 
  • Serves as scientific liaison to other facilities and departments and scientific/quality control member of the Material Review Board.
  • Assists with appropriate review of analytical results of completed raw material, stability samples, and finished product testing. 
  • Reviews and approves laboratory investigations, corrective and preventive actions, change requests, and deviations as necessary.
  • Maintain equipment calibration schedule and ensure that all required calibrations and maintenance are completed in a timely fashion.
  • Author SOP's and assist with the revision process of current procedures.
  • Ensure pharmaceutical laboratory compliance with applicable regulations. 
  • Assist with procedural, cGMP, and safety training of laboratory staff.
  • Assist with preparations for internal and external (including FDA) laboratory audits and inspections.
  • Administers annual laboratory budget and other related duties as required.

REQUIRED SKILLS, ABILITIES, AND QUALIFICATIONS:
  • Bachelor's or higher degree in Chemistry or related discipline.
  • 10+ years of experience in a pharmaceutical QC or Analytical chemistry laboratory.
  • Experience with semi-solid and liquid pharmaceutical environment.  
  • 3+ years of experience in GLP or GMP (preferred) environment.
  • Strong leadership experience, team of 4 or more
  • Strong communication with the ability to build relationships at all levels of the organization.
  • Ability to organize, prioritize, and effectively perform concurrent tasks with minimal supervision.

Estimated Min Rate: $73500.00
Estimated Max Rate: $105000.00
What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:
  • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
  • Health Savings Account (HSA) (for employees working 20+ hours per week)
  • Life & Disability Insurance (for employees working 20+ hours per week)
  • MetLife Voluntary Benefits
  • Employee Assistance Program (EAP)
  • 401K Retirement Savings Plan
  • Direct Deposit & weekly epayroll
  • Referral Bonus Programs
  • Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice

Company Description

Yoh delivers expertise, methodology, and momentum to keep work moving forward. From strategy to execution, we deliver bold ideas and big results through consulting, staffing, and enterprise solutions. Nearly a century after our founding, Yoh remains STEM-centered, collaborative, and committed to client success. Yoh is a proud member of the Day & Zimmermann family of companies. Visit us at https://www.yoh.com/