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Temporary 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 ...

Candidates with strong analytical chemistry, chromatography, and pharmaceutical QC laboratory experience are highly encouraged to apply. Key Responsibilities * Perform analytical testing for incoming ...

Interest in building a long-term career in pharmaceutical quality control or analytical chemistry ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

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 ...

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 ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

Antheia is the advanced biosynthesis company transforming pharmaceutical manufacturing and ... Part-time ( temporary roles are not eligible for Company sponsored benefits. * Comprehensive ...

$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 ...

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Temporary Pharmaceutical Quality Control information

What is the difference between Temporary Pharmaceutical Quality Control vs Permanent Pharmaceutical Quality Control?

AspectTemporary Pharmaceutical Quality ControlPermanent Pharmaceutical Quality Control
CredentialsTypically requires a degree in pharmacy, chemistry, or related field; may need certifications like GMP trainingSame as temporary; often requires additional experience or certifications for full-time roles
Work EnvironmentLaboratories, manufacturing sites, quality assurance departmentsSame as temporary; often in similar settings but with more stability
Employment TypeShort-term, contract-based positionsFull-time, permanent roles
Job ResponsibilitiesConduct quality tests, document results, support compliance activitiesSame responsibilities but with increased responsibility and oversight

Temporary Pharmaceutical Quality Control roles provide short-term support in quality testing and compliance, ideal for gaining experience or covering staffing gaps. Permanent roles offer long-term stability, with greater responsibilities and career growth opportunities within the pharmaceutical industry.

What cities are hiring for Temporary Pharmaceutical Quality Control jobs? Cities with the most Temporary 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 Temporary Pharmaceutical Quality Control jobs? States with the most job openings for Temporary 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 6 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/