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Biotech Operations Jobs (NOW HIRING)

Stellar IT Group

BioTech Data Engineer

Saint Louis, MO · On-site

$111K - $133K/yr

Biotech Data Engineer Job Type: FTE Work Mode: Remote The Biotech Data Engineer focuses on ... Partner with analytics, marketing, commercial operations, and core technology/cybersecurity teams ...

PBS Biotech

Supply Chain Specialist

Camarillo, CA · On-site

$38.86 - $49.18/hr

Operations Reports to: Principal Planner, Supply Chain & OperationsAbout PBS Biotech At PBS Biotech, we are advancing the future of cell therapy manufacturing through innovative bioreactor technology.

3 Key Consulting

Engineer, Biotech

Thousand Oaks, CA

$40 - $44/hr

Engineer, Biotech Location: Thousand Oaks, CA. Employment Type: Contract Duration: 12 months with ... the operation and reliability of equipment while driving safety and quality compliance. The ...

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Biotech Operations information

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How much do biotech operations jobs pay per hour?

As of Jun 23, 2026, the average hourly pay for biotech operations in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $30.29 per hour, depending on experience, location, and employer.

What is the difference between Biotech Operations vs Laboratory Technician?

AspectBiotech OperationsLaboratory Technician
Required CredentialsBachelor's degree in biotech, biology, or related field; sometimes certifications in GMP or quality assuranceAssociate's or bachelor's degree in biology, chemistry, or related field; lab safety certifications often preferred
Work EnvironmentManufacturing facilities, quality control labs, production linesResearch labs, clinical labs, testing facilities
Employer & Industry UsageBiotech companies, pharmaceutical manufacturers, biotech startupsResearch institutions, hospitals, biotech and pharma labs

Biotech Operations roles focus on managing production processes, quality assurance, and ensuring compliance in manufacturing settings. Laboratory Technicians primarily perform experiments, testing, and data collection in research or clinical labs. While both roles require scientific knowledge, Biotech Operations emphasizes process management and compliance, whereas Laboratory Technicians focus on hands-on lab work and data analysis.

What are some common challenges faced in Biotech Operations, and how can new team members effectively navigate them?

Biotech Operations professionals often encounter challenges such as stringent regulatory compliance, maintaining production timelines, and managing cross-functional communication between research, quality, and manufacturing teams. New team members can navigate these challenges by proactively seeking mentorship, staying organized with project management tools, and maintaining open communication channels with colleagues in related departments. Embracing a mindset of continuous learning and adaptability is also crucial, as processes and technologies in biotech are constantly evolving.

What are biotech operations?

Biotech operations refer to the management and coordination of processes involved in developing, manufacturing, and distributing biotechnology products. This includes overseeing laboratory research, quality control, regulatory compliance, production scaling, and supply chain logistics. Professionals in biotech operations ensure that products such as pharmaceuticals, vaccines, or genetically engineered organisms are produced safely, efficiently, and in compliance with industry standards. Their work is critical in bringing scientific discoveries from the lab to market and ultimately to patients or consumers.

What are the key skills and qualifications needed to thrive in Biotech Operations, and why are they important?

Thriving in Biotech Operations requires a solid background in life sciences or engineering, experience with regulatory compliance, and a relevant degree such as a B.S. or M.S. in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), quality management systems (QMS), and certifications like Six Sigma or GMP training are highly valuable. Excellent problem-solving abilities, attention to detail, and strong collaboration skills help individuals excel and adapt in dynamic environments. These competencies are essential for ensuring operational efficiency, regulatory adherence, and successful product development in the biotech industry.
More about Biotech Operations jobs
What cities are hiring for Biotech Operations jobs? Cities with the most Biotech Operations job openings:
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What states have the most Biotech Operations jobs? States with the most job openings for Biotech Operations jobs include:
What job categories do people searching Biotech Operations jobs look for? The top searched job categories for Biotech Operations jobs are:
Biotech Operations jobs near you

Technical Writer / Manufacturing SOP Specialist (Biotech Drug Substance Operations)

Inteldot

Barceloneta, PR • On-site

Full-time

Posted 11 days ago

Job description

Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Position Overview
We are seeking experienced Technical Writers / Manufacturing SOP Specialists to support a major initiative within a Biotech Drug Substance Manufacturing Operation in Barceloneta, Puerto Rico. The selected resources will be responsible for the review, revision, optimization, and standardization of manufacturing Standard Operating Procedures (SOPs) and related controlled documentation to support operational excellence, compliance, and process efficiency initiatives at the client site. This is a fully onsite role requiring hands-on collaboration with Manufacturing, Process Engineering, Quality, Validation, and Operations personnel.
Key Responsibilities
  • Review existing manufacturing SOPs, batch records, and operational documentation for accuracy, clarity, compliance, and efficiency
  • Update and optimize procedural documentation in alignment with current manufacturing practices and regulatory requirements
  • Collaborate with Subject Matter Experts (SMEs) across Manufacturing, Quality, Engineering, and Compliance departments
  • Identify opportunities for process simplification and procedural improvements
  • Ensure documentation complies with GMP, FDA, and internal quality standards
  • Support document lifecycle activities including routing, review coordination, version control, and approvals
  • Participate in onsite meetings, walkthroughs, and process observations to capture operational requirements accurately
  • Maintain consistency in formatting, terminology, and technical writing standards across documentation packages

Required Qualifications:
  • Bachelor's degree in science, Engineering, Technical Writing, or related field preferred
  • Minimum of 3-5 years of experience in biotech, pharmaceutical, or regulated manufacturing environments
  • Strong experience reviewing and authoring manufacturing SOPs and controlled GMP documentation
  • Experience supporting Drug Substance manufacturing operations highly preferred
  • Strong technical writing, editing, and document management skills
  • Familiarity with GMP regulations, FDA compliance expectations, and documentation practices
  • Ability to interact effectively with cross-functional teams and manufacturing personnel
  • Strong attention to detail and organizational skills
  • Ability to work independently in a fast-paced manufacturing environment

Preferred Experience
  • Biologics or biotech manufacturing experience
  • Experience with document management systems (Veeva, TrackWise, MasterControl, etc.)
  • Previous experience supporting remediation, optimization, or continuous improvement initiatives
  • Bilingual (English/Spanish) preferred

Work Environment
  • Fully onsite position in Barceloneta, Puerto Rico
  • Manufacturing and operational support environment

Additional Information
  • Candidates must have prior experience supporting similar manufacturing operations and demonstrated expertise in technical writing within regulated biotech or pharmaceutical environments.

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