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Biotech Director Jobs in Puerto Rico (NOW HIRING)

Veg Group

Validation Engineer - Upstream

Humacao, PR · On-site

$70 - $90/hr

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Merck & Co.

The Associate Director, Urology - Oncology Key Accounts is the main point of contact for Our ... biotech, or medical devices)Minimum of 2 years of relevant experience in healthcare, life sciences ...

Mentor Technical Group

Engineer

Juncos, PR · On-site

... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto ... Work under the direct supervision of project managers to complete design, engineering, and ...

Mentor Technical Group

Engineer

Juncos, PR · On-site

$70 - $90/hr

... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto ... Work under the direct supervision of project managers to complete design, engineering, and ...

Veg Group

Engineer

Juncos, PR · On-site

$60 - $80/hr

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Work under the direct supervision of project managers to complete design, engineering, and ...

Kelly Services

Sr Reliability Engineer

Juncos, PR · On-site

$43/hr

How about this one? We're seeking a Sr Reliability Engineer to work at a premier biotechnology ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

Jedson Engineering

Construction Manager

San Juan, PR · On-site

$180 - $260/hr

Organize, lead and direct all construction-related activities related to EPCM projects to ensure ... Site experience- manufacturing and/or engineering experience in support of pharmaceutical, biotech ...

Pinnaql

Engineer

Juncos, PR · On-site

Experience in biotechnology processes, specifically in purification operations. * Knowledge in ... Work under the direct supervision of project managers to complete design, engineering, and ...

Pinnaql

Specialist Tech Engineering

Juncos, PR · On-site

Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Experience in direct process / manufacturing areas. * Must be fully bilingual (English ...

Kelly Services

Senior Validations Engineer

Juncos, PR · On-site +1

$45/hr

Competitive pay with biweekly direct deposit (W-2) * Hands-on experience supporting critical manufacturing and quality systems in a leading biotechnology environment * Collaborative, fast-paced, and ...

Quality Consulting Group

JT630 - SR ENGINEER

Juncos, PR · On-site

$102K - $140K/yr

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Define system boundaries and identify direct/indirect impact systems. * Lead risk assessments (e.g ...

Pinnaql

Engineering Technical Leads ETL

Juncos, PR · On-site

Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Must be fully bilingual (English / Spanish) with excellent oral skills. * Strong knowledge in ...

Kelly Services

Senior Reliability Engineer

Juncos, PR · On-site

$44/hr

Experience in pharmaceutical, biotechnology, or other highly regulated manufacturing environments ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

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Biotech Director information

What does a Biotech Director do?

A Biotech Director oversees research, development, and operational strategies in a biotechnology company or department. They manage teams, ensure regulatory compliance, and drive innovation to develop new products or therapies. Responsibilities often include budgeting, partnerships, and aligning company goals with scientific advancements. Strong leadership, technical expertise, and industry knowledge are essential for success in this role.

What are the key skills and qualifications needed to thrive as a Biotech Director?

To thrive as a Biotech Director, you need advanced expertise in biotechnology, project management, and leadership, usually demonstrated by a relevant advanced degree and substantial industry experience. Familiarity with laboratory information management systems (LIMS), regulatory compliance protocols (such as FDA or EMA), and certifications like PMP or Six Sigma are highly valued. Excellent communication, problem-solving, and team-building skills help Biotech Directors effectively coordinate multidisciplinary teams and drive innovation. These skills and qualities ensure projects are completed efficiently, regulatory standards are met, and company goals in research and product development are achieved.

What are some common challenges faced by Biotech Directors and how are they addressed?

Biotech Directors often encounter challenges such as balancing regulatory compliance with innovation, managing cross-functional teams, and adapting to fast-paced advancements in technology. Addressing these issues requires staying informed on industry regulations, fostering a culture of open communication, and implementing effective project management strategies. Directors typically work closely with scientists, regulatory specialists, and business development teams to align project timelines, budgets, and objectives. Overcoming these challenges is a rewarding aspect of the role and helps drive organizational success in a competitive industry.

What are the most commonly searched types of Biotech jobs in Puerto Rico?

The most popular types of Biotech jobs in Puerto Rico are:

What are popular job titles related to Biotech Director jobs in Puerto Rico?

For Biotech Director jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Biotech Director jobs in Puerto Rico look for?

The top searched job categories for Biotech Director jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Biotech Director jobs?

Cities in Puerto Rico with the most Biotech Director job openings:

Biotech Director jobs near you
Infographic showing various Biotech Director job openings in Puerto Rico as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% In-person job distribution.

Validation Engineer - Upstream

Veg Group

Humacao, PR • On-site

$70 - $90/hr

Other

Posted 5 days ago

Job description

Current job opportunities are posted here as they become available.

Validation & Engineering Group, Inc. (V&EG), a Pinnaql company, is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in areas such as Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Description

We are seeking a Validation Engineer with experience in upstream equipment to join our team. The Validation Engineer will be responsible for validating equipment, processes, and systems used in the manufacturing process to ensure compliance with industry standards and regulations. Knowledge of common upstream equipment in biotech is a plus.

Qualifications
  • Bachelor's degree in Engineering or related field.
  • Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.
  • Proven experience as a Validation Engineer in a manufacturing environment.
  • Strong knowledge of upstream equipment and processes, including but not limited to: fermenters, bioreactors, centrifuges, filtration systems, and chromatography equipment.
  • Familiarity with industry regulations and standards.
  • Excellent problem-solving skills and attention to detail.
  • Effective communication skills and ability to work in a team environment.
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
  • Available to work extended hours, possibility of weekends and holidays.
Responsibilities
  • Develop and execute validation protocols for equipment and processes.
  • Coordinate with cross-functional teams to ensure validation requirements are met.
  • Analyze validation test results and prepare reports documenting findings.
  • Identify and address deviations or non-conformances during the validation process.
  • Support continuous improvement initiatives related to equipment validation.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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