QC Microbiologist

TekWissen LLC; Portsmouth (NH); On-site; USD 42,000 - 62,000; Full time

Job summary

TekWissen Group is seeking an entry-level QC Microbiologist to support in-process and final product testing, as well as stability studies. The role requires adherence to cGMP and data integrity standards, with responsibilities spanning sample testing, data entry, and quality checks at the Portsmouth facility.

Qualified candidates will have a high school diploma (associate degree preferred) and 0–4 years of lab experience.

Qualifications

• Entry-level QC/Lab experience: 0–4 years.
• Knowledge of cGMP and data integrity principles.
• Ability to interpret data independently and with guidance.
• Strong written and verbal communication skills.
• Ability to follow instructions and procedures.

Responsibilities

• Run test samples for In-Process, Lot Release, and Stability studies.
• Support Utility and HVAC monitoring and sampling.
• Use Microsoft Word, Excel, and PowerPoint.
• Use laboratory computer systems.
• Apply Data Integrity principles per policies and procedures.
• Complete assigned tasks accurately and on time.
• Work effectively as an active member of the team.
• Adhere to cGMPs during API manufacture.
• Notify management of inspections, deviations, and defects.
• Follow required health and safety training.
• Promote workplace safety and report incidents.
• Comply with site and company safety policies.
• Work the full shift and arrive on time.
• Perform other duties as assigned.

Skills

Data interpretation

Quality control

Critical thinking

Team collaboration

Communication

Problem-solving

Attention to detail

Self-motivated

Education

High School Diploma or equivalent

Associate's Degree in Microbiology/Biochemistry or related field

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 Microbiologist

Location:

Portsmouth, NH 03801

Duration:

8 Months

Job Type:

Temporary Assignment

Work Type:

Onsite

Summary:

The Quality Microbial Control Analyst I / QC Microbiologist will act as a team member of the Quality Microbial Control department to support production of in-process and final product drug lots and quality testing for ongoing customer stability studies. The role provides on-time, high-quality results to meet manufacturing demands and applies job skills, policies, and procedures to complete a variety of tasks. The position is entry-level and involves semi-routine assignments requiring the ability to recognize deviations from accepted practices and work on problems of moderate scope.

Responsibilities:

• Run test samples for In-Process, Lot Release, and Stability studies.
• Support Utility and HVAC monitoring and sampling throughout the facility.
• Use Microsoft Word, Excel, and PowerPoint.
• Use laboratory computer systems.
• Apply Data Integrity principles in all aspects of work in compliance with applicable policies, guidelines, and procedures.
• Apply job skills, policies, and procedures to complete assigned tasks.
• Recognize deviations from accepted practices and determine appropriate action within defined procedures and practices.
• Complete assignments accurately and on time.
• Work effectively as an active member of the team.
• Maintain commitment to quality and perform job functions to the best of one's ability.
• Adhere to cGMPs at all times during the manufacture of APIs.
• Take responsibility for the quality of work delivered and promptly notify management of regulatory inspections, serious GMP deficiencies, process deviations, product defects, and related actions.
• Follow job safety procedures and attend required health and safety training.
• Proactively promote workplace safety and promptly report actual and potential accidents and injuries.
• Comply with site and company safety policies.
• Work the entire assigned shift, including arriving on time.
• Perform other duties as assigned.

Required Skills:

• High School Diploma or equivalent required.
• Associate's Degree preferred, preferably in Microbiology, Biochemistry, or a related science field.
• Entry-level Quality Control/Laboratory experience: 0 4 years.
• Strong ability to interpret data independently and with guidance.
• Ability to perform assigned complex and/or varied tasks.
• Prioritization and problem-solving skills.
• Ability to comprehend and follow instructions.
• Strong written and verbal communication skills.
• Ability to exercise judgment within defined procedures and practices to determine appropriate action.
• Ability and desire to learn from experience.
• Ability to treat errors as learning opportunities.
• Ability to work effectively as a self-motivated team player.
• Ability to relate to others in a team setting.
• Ability to complete assignments accurately and on time.
• Commitment to quality.
• Ability to understand internal and/or external customer needs.
• Ability to monitor KPIs with the supervisor and consistently deliver goals.
• Ability to take responsibility for personal and team safety.
• Knowledge and adherence to cGMP requirements.
• Understanding and application of Data Integrity principles.

TekWissen Group is an equal opportunity employer supporting workforce diversity.