1

Qc Biotech Jobs in Atkinson, NH (NOW HIRING)

QC Analyst IV

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Analyst IV Location: Portsmouth, NH 03801 Duration: 8 Months Job Type: Temporary ...

Minimum of 3+ years of experience in a GMP, pharmaceutical, biotechnology, environmental, microbiology, or quality control laboratory environment * Experience performing laboratory testing and ...

Minimum of 3+ years of experience in a GMP, pharmaceutical, biotechnology, environmental, microbiology, or quality control laboratory environment * Experience performing laboratory testing and ...

QC Analyst III

Portsmouth, NH · On-site

$25 - $30/hr

Our client is a leading biotechnology company that combines technological expertise with world ... Job Title: QC Analyst III Location: Portsmouth, NH 03801 Duration: 12 months Job Type: Temporary ...

Quality Control Technician

Tewksbury, MA · On-site

$17 - $17.25/hr

The job opportunity below is with one of our clients specializing in biotechnology product ... Quality Control Technician Location: Tewksbury, MA 01876 Duration: 12 Months Job Type: Temporary ...

Quality Control Technician

Tewksbury, MA · On-site

$20.25 - $25.75/hr

The job opportunity below is with one of our clients specializing in biotechnology product ... Quality Control Technician Location: Tewksbury, MA 01876 Duration: 12 Months Job Type: Temporary ...

Job Title: QC Senior Scientist - Raw Materials Location: Portsmouth, NH (On-site) As a QC Scientist ... Experience in a GMP-regulated laboratory, pharmaceutical, biotechnology, or related environment ...

Job Title: QC Senior Scientist - Raw Materials Location: Portsmouth, NH (On-site) As a QC Scientist ... Experience in a GMP-regulated laboratory, pharmaceutical, biotechnology, or related environment ...

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not ... Provides support to manufacturing by delivering samples to the QC laboratories. The qualified ...

next page

Showing results 1-20

Qc Biotech information

See Atkinson, NH salary details

$29.7K

$79.1K

$125.9K

How much do qc biotech jobs pay per year?

As of Sep 1, 2026, the average yearly pay for qc biotech in Atkinson, NH is $79,069.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,800.00 and $97,200.00 per year, depending on experience, location, and employer.

What is a QC Biotech?

A QC (Quality Control) Biotech professional is responsible for ensuring that biotechnology products, such as pharmaceuticals, vaccines, or biologics, meet strict quality and safety standards. They perform laboratory tests, analyze samples, and document results to ensure compliance with regulatory guidelines. QC Biotech professionals play a crucial role in maintaining the integrity of products before they reach the market, working closely with other departments to resolve any quality issues. Their work helps protect patient safety and supports the success of biotech companies.

What are the key skills and qualifications needed to thrive as a QC Biotech?

To thrive as a QC Biotech, you need a solid background in biology, chemistry, and laboratory techniques, usually supported by a degree in life sciences or a related field. Familiarity with analytical instruments such as HPLC, PCR, and ELISA, as well as GMP regulations and LIMS software, is typically required. Attention to detail, strong problem-solving abilities, and effective teamwork are crucial soft skills for this role. These skills and qualities ensure accurate testing, regulatory compliance, and the integrity of biotechnological products.

What are some common challenges faced by QC Biotech professionals and how can they be addressed?

QC Biotech professionals often encounter challenges such as adapting to rapidly changing regulatory standards, troubleshooting complex assay discrepancies, and maintaining precise documentation under tight deadlines. Addressing these challenges requires continuous learning, strong attention to detail, and effective collaboration with cross-functional teams like R&D and manufacturing. Leveraging robust Standard Operating Procedures and clear communication with colleagues can help ensure consistent results and regulatory compliance.

What is the difference between Qc Biotech vs Qc Microbiologist?

AspectQc BiotechQc Microbiologist
Required CredentialsBachelor's in Biology, Biotechnology, or related field; GMP/GxP trainingBachelor's in Microbiology, Biology, or related; microbiology certifications
Work EnvironmentBiotech manufacturing labs, quality control departmentsMicrobiology labs, pharmaceutical or biotech settings
Employer & Industry UsageBiotech companies, pharmaceutical manufacturersPharmaceutical firms, biotech research labs
Common Search & ComparisonYesYes

While both Qc Biotech and Qc Microbiologist roles involve quality testing in biotech and pharmaceutical settings, Qc Biotech focuses on overall product quality, including assays and validation, whereas Qc Microbiologists specialize in microbiological testing and contamination control. The roles often overlap but differ in specific expertise and focus areas.

What cities near Atkinson, NH are hiring for Qc Biotech jobs?

Cities near Atkinson, NH with the most Qc Biotech job openings:

Infographic showing various Qc Biotech job openings in Atkinson, NH as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 6% Part Time, 3% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $79,069 per year, or $38 per hour.

QC Analyst IV

TekWissen LLC

Portsmouth, NH • On-site

$24.50 - $32.75/hr

Temporary

Posted 15 days ago


Job description

Overview:    

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy. 

Job Title:     QC Analyst IV
Location:      Portsmouth, NH 03801 
Duration:      8 Months 
Job Type:       Temporary Assignment 
Work Type:    Onsite 


Summary
The QC Analyst will act as a team member of the Quality Control department to support the production of in-process and final product drug lots for customers. Also participate in quality testing for ongoing customer stability studies while providing on-time, high quality results to meet manufacturing demands. A QC Analyst applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. May be assigned to work on special projects. May also provide support to others in the absence of the supervisor/manager. Works on problems of moderate scope in which analysis of situation or data requires review of identifiable factors. Provides feedback to junior analysts and offers guidance to co-workers with respect to compliance.

Responsibilities

  • Delegates tasks to support daily operations.
  • Responsible for the state of equipment in the laboratory, working with maintenance, calibration, and vendors to ensure their activities are accomplished and the equipment is ready for next use.
  • Equipment may include but is not limited to, pH/conductivity meters, Agilent and Waters HPLC systems, UPLC systems, pipettes, SoloVPE and Cary 60 spectrophotometers, PA-800 capillary electrophoresis instruments, Protein Simple iCE3/icIEF instruments, 7500 Real Time PCR systems, KingFisher Flex instruments, Sysmex CS-2500 instruments and include quality review of quality and vendor binders.
  • Troubleshoot equipment and software as necessary.
  • Will train for assay execution and review within the HPLC Analytical Lab and Electrophoresis lab and have ability to cross train into Immunology as applicable.
  • Has the ability to get trained to run and review advanced assays as necessary.
  • Identifies areas of improvement and works to implement them, including 6S, document revisions, workorders, and change controls.
  • Communicates to other departments as appropriate, including MFG, QA, and MSAT, during operations and escalate issues as needed.
  • Initiates and assists with investigations as required within the job functions.
  • Drives audit readiness on the team with advanced regulatory knowledge.
  • Conduct Pre-Audit walks through the laboratory space.
  • Available to confidently and competently speak to auditors as QC SME.
  • Apply Data Integrity principles in all aspects of work, in compliance with DI policies, guidelines and procedures.
  • Completes assigned tasks on-time and accurately.
  • Can identify needed tasks and complete without direction.
  • Perform other duties as assigned.
  • Adherence to cGMPs is required at all times during the manufacture of APIs.
  • All personnel own the quality of what they deliver and are responsible for notifying management in a timely manner of regulatory inspections, serious GMP deficiencies, process deviations, product defects and related actions.

Required Skills

  • Bachelor's Degree.
  • Biochemistry or Related Science Fields.
  • A combination of education and years of experience will be considered.
  • Comprehend and follow instructions.
  • Exercises judgement within defined procedures and practices to determine appropriate action.
  • Strong ability to interpret data both alone and with guidance.
  • Works entire assigned shift, including arriving on time.
  • Timeliness in completing assigned tasks.
  • Strong communication skills, both written and verbal format.
  • Self-motivated team player, relate to others in a team environment.
  • Maintain a positive and professional attitude within the team environment.
  • Completes assignments on-time and accurately, with minimal re-work.
  • Displays commitment to quality and performs job functions to the best of their ability.
  • Perform assigned, complex and/or varied tasks.
  • Prioritization and problem solving.
  • Direct, control and plan tasks/projects.
  • Brainstorming.


TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity. 


TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 


TekWissen logo

About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media