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Trainee Biotechnology Jobs (NOW HIRING)

Curia, Inc.

Training Program Manager

Rensselaer, NY · On-site

$114K - $142K/yr

... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ... Collect and analyze trainee feedback to identify improvement opportunities * Recommend and ...

AMRI

Training Program Manager

Rensselaer, NY

$114K - $142K/yr

... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ... Collect and analyze trainee feedback to identify improvement opportunities * Recommend and ...

BMWC CONSTRUCTORS

Training Coordinator

Indianapolis, IN · On-site

Communicate with trainees, supervisors, internal and external training partners, and other vendors ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

BMWC CONSTRUCTORS

Training Coordinator

Indianapolis, IN · On-site

Communicate with trainees, supervisors, internal and external training partners, and other vendors ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

BMWC Constructors

Training Coordinator

Indianapolis, IN · On-site

Communicate with trainees, supervisors, internal and external training partners, and other vendors ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

Wisconsin

Neuroradiologist

Madison, WI · On-site

We provide an environment for education of our trainees, staff, and healthcare professionals ... Phase 2 of the Wisconsin Biotech hub was announced in July 2024, resulting in $49 million in ...

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Trainee Biotechnology information

See salary details

$25.5K

$43.5K

$63.5K

How much do trainee biotechnology jobs pay per year?

As of Jul 1, 2026, the average yearly pay for trainee biotechnology in the United States is $43,530.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $51,000.00 per year, depending on experience, location, and employer.

What types of projects or tasks can a Trainee in Biotechnology expect to work on during their initial months?

As a Trainee in Biotechnology, you can expect to be involved in a variety of hands-on and support tasks such as assisting with laboratory experiments, preparing samples, analyzing data, and maintaining lab equipment. You may also participate in ongoing research projects under the supervision of senior scientists, gaining exposure to techniques like PCR, gel electrophoresis, or cell culture. Collaboration with cross-functional teams, such as quality control and research & development, is common, providing valuable insights into different areas of biotechnology. These experiences help you build foundational lab skills and understand the workflow of a professional biotech environment.

What are the key skills and qualifications needed to thrive as a Trainee in Biotechnology, and why are they important?

To thrive as a Trainee in Biotechnology, a strong foundation in biological sciences, laboratory techniques, and a relevant degree (such as biotechnology, biology, or biochemistry) is essential. Familiarity with laboratory equipment, molecular biology tools, and software for data analysis, as well as safety certifications, is typically required. Attention to detail, problem-solving ability, and effective communication are standout soft skills in this role. These skills and qualities are crucial for ensuring accurate experimental results, maintaining lab safety, and contributing effectively to research and development teams.

What is the difference between Trainee Biotechnology vs Laboratory Technician?

AspectTrainee BiotechnologyLaboratory Technician
Required CredentialsTypically pursuing or completed a degree in Biotechnology or related fieldAssociate degree or diploma in Laboratory Technology or related field
Work EnvironmentTraining programs, research labs, biotech companiesOperational labs, research facilities, quality control labs
Employer & Industry UsageEntry-level training roles in biotech firms, research institutionsTechnical roles in labs across healthcare, pharmaceuticals, biotech

In summary, a Trainee Biotechnology is an entry-level position focused on gaining practical experience in biotech environments, often requiring ongoing education. A Laboratory Technician is a more established role requiring specific technical certifications, responsible for conducting experiments and maintaining lab operations. Both roles are essential in the biotech industry but differ mainly in experience level and responsibilities.

What are trainee biotechnology professionals?

Trainee biotechnology professionals are individuals who are starting their careers in the biotechnology field, often participating in structured training or internship programs. They work under supervision to learn laboratory techniques, data analysis, and industry-specific regulations. Their responsibilities may include supporting research and development, assisting with experiments, and gaining hands-on experience with biotechnology tools and processes. This role serves as a stepping stone for advanced positions in research, quality control, or product development within the biotech industry.
What cities are hiring for Trainee Biotechnology jobs? Cities with the most Trainee Biotechnology job openings:
What are the most commonly searched types of Biotechnology jobs? The most popular types of Biotechnology jobs are:
What states have the most Trainee Biotechnology jobs? States with the most job openings for Trainee Biotechnology jobs include:
What job categories do people searching Trainee Biotechnology jobs look for? The top searched job categories for Trainee Biotechnology jobs are:
Trainee Biotechnology jobs near you
Infographic showing various Trainee Biotechnology job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, 7% Part Time, and 1% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $43,530 per year, or $20.9 per hour.

MDI - Documentation Specialist Trainee - Production

Cipla

Fall River, MA • On-site

$66K - $70K/yr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago

Job description

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates
Job Title: MDI - Documentation Specialist Trainee - Production
Employment Type: Full Time / Exempt
Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
Salary Range: $66,300-$70,000
Job Overview
The Manufacturing Documentation Specialist is responsible for the creation and revision of new and existing GMP batch production records as well as SOP's. In this role, the Documentation Specialist adheres to the company's document and SOP's procedures while ensuring their accuracy, quality, and integrity.
The job duties for this position include but are not limited to the following:
  • Works with Manufacturing/Packaging to deliver timely batch record review across all shifts.
  • Reviews and approval of master batch records.
  • Develops appropriate disposition metrics, works with manufacturing/packaging personnel to achieve said targets. Generates and reports on metrics on agreed frequency
  • Creates training materials for subject matter input.
  • Track and manage periodic review of approved procedures.
  • Develop strategies and documents for cleaning and process validation of equipment and products in compliance with site SOPs and regulatory guidance.
  • Provides data to support management evaluation of performance trends
  • Owns quality records (change control, CAPA's, deviations) and delivers to established timelines.
  • Autonomously leads and manages projects to implement continuous improvement opportunities.
  • Lead and/or support root cause investigations related to performance trends and formal deviations.
  • Develop, implement and assess solutions for complex problems.
  • Anticipates risk and builds contingencies to help mitigate impact.
  • Reviews document for accuracy and completeness.
  • Defends the validation programs and strategies to customers and regulatory auditors.
  • Performs weekly quality reviews of Master Control database by assuring new documents have been entered using appropriate protocols.
  • Follows strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Manufacturing Practices (cGMP), complying with legal regulations, monitoring the environment.
  • Performs other duties as assigned.
Education and Experience
  • Associate degree with 1-3 years knowledge and experience of GMP documentation required.
  • Bachelor's degree in science, biochemistry, pharmaceutical engineering, Pharmaceutical Sciences, or related discipline from an accredited college/university preferred.
  • Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study from an accredited college/university preferred.
  • Minimum one (1) year documentation experience and three (3) years related pharmaceutical or biotech industry experience. Preference will be given to candidates with experience in generic pharmaceutical manufacturing.
Technical Knowledge and Computer Systems Skills
  • Proficient in Microsoft Office Suite, with intermediate skills in Word and Excel.
  • Strong organizational and time-management skills with the ability to prioritize multiple tasks in alignment with departmental and site-wide objectives.
  • Ability to work independently as a self-starter and collaboratively within a dynamic, cross-functional, team-based environment.
  • Demonstrated attention to detail, strong analytical skills, and solid basic math proficiency.
  • Ability to read, write, and communicate effectively in English.
  • Flexible and adaptable, with the ability to thrive in a fast-paced manufacturing environment and adjust quickly to changing priorities and schedules.
GMP, Compliance, and Quality Systems Knowledge
  • Working knowledge of pharmaceutical manufacturing operations and associated documentation.
  • Knowledge and hands-on experience with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and strict adherence to internal protocols and Standard Operating Procedures (SOPs).
  • Experience writing, revising, and creating cGMP records, SOPs, batch records (BMR/eBMR), eLogbooks, and documentation templates.
  • Knowledge and handling of deviations, CAPAs, change controls, FMECA, OOS, OOT, training records, and OOAC.
  • Experience supporting compliance activities, including participation in local and federal regulatory audits.
  • Ability to facilitate problem solving and root cause investigations, and to develop, implement, and assess solutions to complex issues.
  • Responsible for closure of compliance-related CAPAs.
Systems, Data, and Planning
  • Experience with electronic quality and document management systems such as SAP, MasterControl, and TrackWise preferred.
  • Ability to understand, analyze, and interpret complex data sets; experience with statistical analysis tools is a plus.
  • Knowledge of batch planning and execution in accordance with production plans

Benefits
In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance -medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid and unpaid family leave, employee discounts, and other benefits.
About Cipla
Cipla is a leading global pharmaceutical company dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Driven by the purpose of 'Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.
In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division.
InvaGen Pharmaceuticals, Inc.
InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States.
Equal Opportunity Employer
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter.
About the Salary/ Pay Range
The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

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