QC Scientist, I - Method Validation(W)

Cellipont Bioservices; The Woodlands (TX); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

401K employer match

Tuition Reimbursement

Flexible work schedules

Paid holidays

Job summary

Cellipont Bioservices is seeking a QC Scientist I to support the quality control department with analytical method qualification/validation for cell therapy products in a GMP setting. You will independently execute complex laboratory work and prepare technical documentation, ensuring timely and cost-effective results.

The role requires cross-functional collaboration with QA, AD, manufacturing, and PD teams, plus hands-on experience in flow cytometry, cell-based assays, and GMP environments.

Qualifications

• B.S. in Biology, Biochemistry, Biotechnology, Immunology, Microbiology or related field; Master’s degree preferred.
• Minimum 4 years in biotechnology, pharmaceutical, or cell therapy with analytical method qualification/validation experience.
• Hands-on mammalian cell culture and aseptic technique in GMP environment.
• Experience with flow cytometry, potency, viability, and molecular assays is preferred.
• Strong self-starter with ability to meet client deadlines under minimal supervision.

Responsibilities

• Execute analytical method qualification and validation studies for release, stability, characterization and in-process testing in GMP.
• Independently perform cell-based assays including potency, flow cytometry, viability, proliferation and cytotoxicity.
• Support transfer of commercial methods and method validation into QC per regulatory requirements.
• Generate and document data following GMP, GDP, ALCOA+ requirements.
• Present findings and assist in preparing technical reports and client presentations.

Skills

Flow cytometry

Mammalian cell culture

Analytical method validation

qPCR / PCR techniques

ELISA assays

GMP/GLP knowledge

Education

B.S. in Biology or related science

Master's preferred

Tools

Cell culture techniques

Analytical instrumentation

Job description

Job Summary

Cellipont Bioservices is growing, and we are looking for a QC Scientist I, who believes in the potential of bridging clients discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QC Scientist I works in a fast-paced environment supporting the quality control department cell therapy analytical method qualifications and validations. The QC Scientist I will be responsible for independent execution of complex laboratory/experiment work with a high degree of technical proficiency focused on method qualification and/or validation within a GMP environment, QC document preparation and revision (SOPs/Protocols/Reports), as well as technical support for QC lab investigations. The QC Scientist I is also responsible for ensuring all activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will require the individual to demonstrate strong ability to work cross-functionally and possess strong leadership skills.

The Role

• Execute analytical method qualification and validation studies supporting release, stability, characterization and in process testing of cell therapy products in a GMP environment.
• Independently perform cell-based assays, including potency, flow cytometry, viability, proliferation, cytotoxicity, ELISA, and molecular PCR testing methods, among others.
• Support transfer of commercial methods and method validation into QC in compliance with regulatory requirements.
• Generate, review, and document analytical data following GMP, GDP, ALCOA+, and regulatory compliance requirements.
• Present experimental findings and support preparation of technical reports and presentations to clients.
• Provide technical expertise on bioassay, flow cytometry and/or molecular biology methods in support of QC lab investigations, to identify root cause and provide corrective and preventative actions, if needed.
• Prepare and revise method qualification/validation protocols, technical reports SOPs, and laboratory documentation supporting analytical method lifecycle management.
• Evaluate assay performance characteristics including accuracy, precision, specificity, robustness, and suitability for intended analytical applications.
• Collaborate with QA, Analytical Development (AD), Manufacturing and Process Development (PD) teams to support compliant analytical testing programs.
• Work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects.
• Communicate effectively with cross-functional peers, department management, and other partners as needed.

The Candidate

• B.S. in Biology, Biochemistry, Biotechnology, Immunology, Microbiology, or related scientific discipline, or Master's Degree preferred
• Minimum 4 years of experience in biotechnology, pharmaceutical or cell therapy experience required. Previous experiment in analytical method qualification/validation is a must.
• Hands-on experience with mammalian cell culture and aseptic techniques in a laboratory and/or GMP environment.
• Experience performing analytical methods including flow cytometry, cell-based potency, viability, proliferation, cytotoxicity, ELISA or molecular assays preferred.
• Self-starter with the ability to produce results in a fast-paced environment to meet client deadlines under minimal supervision.
• Hands-on experience with analytical method transfers/qualifications/validations is a plus.
• Technical background and expertise in flow cytometry is a plus.
• Knowledge of cGMP/ICH/FDA regulations.
• Excellent oral and written communication skills.

Position Benefits

• Opportunities for career growth within an expanding team
• Defined career path and annual performance review & feedback process
• Cross-functional exposure to other areas of within the organization
• Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members
• 401K strong employer match
• Tuition Reimbursement
• Employee Referral Bonuses
• Flexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidays
• Gain experience in the cutting-edge cell therapy space

At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!

Notice to Agency and Search Firm Representatives

Cellipont Bioservices is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.c