Quality Control Scientist I

TekWissen ®; Cincinnati (OH); On-site; USD 34,000 - 43,000; Full time

Job summary

TekWissen is assisting a biotechnology client in Cincinnati with a temporary assignment for a Quality Control Scientist I. The role focuses on reviewing analytical data from QC laboratories, raw materials, in-process samples, finished products, and stability studies.

The ideal candidate has a chemistry/biology background, 2+ years in regulated environments, proficiency with HPLC, GC, spectroscopy, and a strong commitment to GMP and data integrity; onsite First Shift, 12-month duration, pay $25

Qualifications

• Bachelor's degree in Chemistry, Biology, Biochemistry, Microbiology, or related science field.
• 2+ years of laboratory experience in regulated environments preferred.
• Experience with data review and analytical testing.
• GMP regulations, Good Documentation Practices, and data integrity knowledge.
• QC laboratory or regulated testing experience preferred.
• Strong attention to detail and ability to evaluate scientific data.
• Strong analytical, organizational, and communication skills.
• Proficiency with Microsoft Office and LIMS.
• Ability to work independently and collaboratively.
• Commitment to quality, safety, compliance and data integrity.

Responsibilities

• Review analytical data, lab records and supporting documentation from QC labs.
• Review data from HPLC, GC, spectroscopy, dissolution testing and wet chemistry.
• Verify calculations, results, specs, instrument outputs and chromatograms.
• Ensure lab records comply with SOPs, GMP and data integrity standards.
• Identify errors and discrepancies; collaborate to resolve.
• Review data for raw materials, in-process, finished products and stability studies.
• Use LIMS and electronic systems to track data and sample status.
• Support investigations, deviations and OOS/OOT events as needed.
• Maintain traceable records per data integrity requirements.
• Collaborate with QC, QA, and cross-functional teams to meet timelines.
• Follow safety, quality, regulatory and site procedures.

Skills

Attention to detail

Data analysis

QA data review

GMP knowledge

Documentation skills

Communication skills

Independent work

Team collaboration

LIMS familiarity

HPLC

GC

Spectroscopy

Dissolution testing

Wet chemistry

Data integrity

Education

Bachelor's degree in Chemistry/Biology/Biochemistry/Microbiology

Tools

LIMS

Microsoft Office

Job description

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to clients worldwide. The job opportunity below is with one of our clients specializing in biotechnology product development services. The client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As a global leader in serving the scientific community, the organization generates approximately $40 billion in annual revenue and is committed to making the world healthier, cleaner, and safer. Their global team delivers innovative technologies, convenient procurement solutions, and pharmaceutical services through industry-leading brands.

Position: Quality Control Scientist I

Duration: 12 Months

Job Type: Temporary Assignment

Work Type: Onsite

Shift: First Shift

Pay Ragne: $25 to $31

Summary:

The Data Review Scientist / Quality Control Scientist I will review analytical testing data associated with raw materials, in-process samples, finished products, and stability samples. The ideal candidate will have strong attention to detail, scientific judgment, and the ability to identify and resolve data or documentation discrepancies. The position requires experience in a chemistry, biology, microbiology, or biochemistry laboratory, preferably within a pharmaceutical, biotechnology, or other regulated environment.

Responsibilities:

• Review analytical data, laboratory records, and supporting documentation generated by QC laboratories.
• Review data from analytical techniques including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry.
• Verify calculations, results, specifications, instrument outputs, chromatograms, and associated documentation for accuracy and completeness.
• Ensure laboratory records comply with approved methods, specifications, SOPs, GMP requirements, and Good Documentation Practices.
• Identify errors, discrepancies, atypical results, and documentation deficiencies and work with laboratory personnel to facilitate resolution.
• Review data associated with raw materials, in-process samples, finished products, and stability studies.
• Utilize LIMS and other electronic laboratory systems to review and track analytical data and sample status.
• Support investigations, deviations, OOS/OOT events, and other quality activities as assigned.
• Maintain accurate and traceable records in accordance with applicable data integrity requirements.
• Collaborate with QC analysts, laboratory leadership, Quality Assurance, and other cross-functional teams to support testing and product-release timelines.
• Follow applicable safety, quality, regulatory, and site procedures.

Required Skills:

• Bachelor's degree in Chemistry, Biology, Biochemistry, Microbiology, or a related scientific field.
• 2+ years of relevant laboratory experience preferred, ideally within a pharmaceutical, biotechnology, or other regulated environment.
• Experience with laboratory data review and/or analytical laboratory testing preferred.
• Working knowledge of analytical techniques such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry.
• Knowledge of GMP regulations, Good Documentation Practices, pharmaceutical quality standards, and data integrity principles is required.
• Experience working in a QC laboratory or regulated testing environment is highly preferred.
• Strong attention to detail and ability to critically evaluate scientific data and identify discrepancies.
• Strong analytical, problem-solving, organizational, written, and verbal communication skills.
• Proficiency with Microsoft Office and laboratory information/electronic data systems such as LIMS.
• Ability to work independently and collaboratively in a dynamic environment.
• Strong commitment to quality, safety, compliance, and data integrity.

TekWissen® Group is an equal opportunity employer supporting workforce diversity.