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Sr. Scientific Support Specialist – Manufacturing Media/Buffer Prep Specialist

Thermo Fisher Scientific
Thermo Fisher Scientific
2-5 years
preferred by company
10 Dec. 26, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Scientific Support Specialist – Manufacturing Media & Buffer Preparation

Job ID: R-01331800
Employment Type: Full-Time
Work Mode: Fully Onsite
Location: Thousand Oaks, California, United States
Category: Clinical Research | Laboratory Manufacturing | Scientific Operations
Experience Required: 2–5 years
Work Schedule: Standard (Monday to Friday)


About the Organization

Our Clinical Research Services team supports the development of life-changing therapies by delivering high-quality scientific, technical, and operational expertise. As part of a leading global Contract Research Organization (CRO), the team contributes to the PPD® clinical research portfolio and partners closely with Thermo Fisher Scientific to accelerate drug development and improve patient outcomes worldwide.

Thermo Fisher Scientific’s mission is to enable customers to make the world healthier, cleaner, and safer by advancing research, development, and manufacturing across the life sciences industry.


Role Overview

The Senior Scientific Support Specialist – Manufacturing Media/Buffer Prep Specialist is a critical onsite role within Unity™ Lab Services, a division of Thermo Fisher Scientific that provides embedded laboratory and manufacturing support at customer sites globally.

This position is responsible for preparing high-quality media and buffer solutions, supporting pilot plant operations, ensuring regulatory compliance, and delivering operational excellence in a laboratory manufacturing environment.


Key Responsibilities

Laboratory & Manufacturing Operations

  • Prepare media and buffer solutions across a range of volumes and specifications, including multi-kilogram scale

  • Perform pH and conductivity measurements, sterile filtration, and equipment assembly and disassembly

  • Operate, calibrate, and verify laboratory equipment including mixers, pressurized vessels, peristaltic pumps, scales, fume hoods, pH meters, and conductivity meters

  • Follow established SOPs, work instructions, and safety standards to ensure accuracy and compliance

Documentation & Quality Compliance

  • Verify calculations and review technical documentation for accuracy

  • Maintain accurate logbooks, batch records, and manufacturing documentation

  • Scan, archive, and manage laboratory and production records

  • Support audit readiness and regulatory compliance activities

Safety & Continuous Improvement

  • Adhere to laboratory safety requirements, PPE usage, and hazardous material handling protocols

  • Identify opportunities for process improvement and operational efficiency

  • Support continuous improvement initiatives within pilot plant and laboratory operations

Collaboration & Customer Engagement

  • Provide technical guidance, training, and mentorship to colleagues

  • Collaborate with cross-functional teams while maintaining the ability to work independently during high-volume periods

  • Represent Thermo Fisher Scientific professionally at customer sites


Education & Experience Requirements

Education

  • High school diploma or equivalent (required)

  • Associate degree in a scientific discipline (preferred)

Experience

  • Minimum 2+ years of relevant laboratory, manufacturing, or scientific support experience

  • Experience with media preparation, buffer preparation, or laboratory manufacturing operations preferred

  • Prior exposure to GLP/GMP-regulated environments is an advantage


Required Skills & Competencies

  • Strong understanding of laboratory safety, SOP compliance, and quality systems

  • Hands-on experience with laboratory and pilot plant equipment

  • Proficiency in Microsoft Office applications (Outlook, Excel, Word, PowerPoint)

  • Ability to use handheld scanners and electronic data entry systems

  • Strong attention to detail, documentation accuracy, and problem-solving skills

  • Excellent communication and customer service skills

  • Ability to maintain confidentiality and demonstrate professional integrity


Work Environment & Physical Requirements

  • Laboratory and manufacturing environment with exposure to hazardous or toxic materials

  • Ability to lift up to 40 lbs without assistance; occasional lifting up to 50 lbs

  • Use of PPE including lab coats, safety glasses, gloves, gowns, masks, and steel-toe footwear

  • Flexible scheduling may be required, including evenings, weekends, or rotating shifts

  • Potential exposure to chemical-based allergens


Compensation & Benefits

  • Estimated hourly pay range (California): USD 21.82 – 26.50, based on experience and qualifications

  • Eligibility for variable annual bonus programs as per company policy

  • Comprehensive total rewards package including:

    • Medical, dental, and vision insurance plans

    • Paid time off, paid holidays, and parental leave

    • Employee assistance programs and tuition reimbursement

    • Retirement savings plans and employee stock purchase program


Why Join This Opportunity?

This role offers hands-on exposure to advanced laboratory manufacturing operations within a globally recognized life sciences organization. You will contribute directly to scientific innovation, patient-focused research, and operational excellence while building a stable and growth-oriented career in clinical research support services.