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Biotech Director Jobs in Puerto Rico (NOW HIRING)

Kelly Services

PR

$38/hr

Experience in manufacturing, process development, or quality assurance within the biotech or ... Competitive pay rate with weekly direct deposit. Bi-Weekly pay by W-2. * Vacations, Sick & Holidays ...

Kelly Services

PR

$65/hr

We're seeking a Sr Packaging Engineer to work at a leading biotech organization in Gurabo, PR . ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

Kelly Services

PR

$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 ...

Kelly Services

PR

$45/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 ...

Quality Consulting Group

PR · On-site

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Review Supplier Statement of Accounts and provide direct feedback and updates to the supplier which ...

Ultimate Solutions

Sr Scientist

Caguas, PR · On-site

$89K - $121K/yr

... biotechnology, medical devices, and logistics markets. Description The successful Sr Validation Scientist will be responsible to Independently provide and/or direct the technical validation ...

MENTOR TECHNICAL GROUP CORP

PR · On-site

Direct supervision and coordination of assigned utilities operators, installers, and mechanics ... Biotechnology, Medical Device, Food and Beverage, and Healthcare) with thorough working knowledge ...

CIS International LLC

PR · On-site

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

Kelly Services

PR

$45/hr

We're seeking a Sr Packaging Engineer to work at a leading biotech organization in Juncos, PR . ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

JC Automation Corp

PR · On-site

Own field HSE leadership in partnership with the HSE Director; enforce LIFE program and BeyondZero ... on pharmaceutical, biotech, or other regulated-industry projects >$500+M TIC. * Track record ...

Weil Group, Inc

PR · On-site

... the direct supervision of project managers to complete design, engineering, and construction ... pharmaceutical/biotech processes Familiarity with validation processes Familiarity with ...

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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 95% In-person, and 5% Remote job distribution.

Specialist Manufacturing (multiple positions)

Kelly Services

PR

$38/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 16 days ago

Job description

At Kelly® Science & Clinical, we’re passionate about helping you find a job that works for you. How about this one? 
We’re seeking for Specialists Manufacturing (multiple positions) to work at a premier biotechnology manufacturing client in Juncos, PR.
Salary: $38.00 hr
Shift: Administrative shift (support a 24/7 manufacturing operations, some remote work is possible)
This job might be an outstanding fit if you have the following requirements:
  • Doctorate OR Master’s degree plus 2 years of Manufacturing Operations experience OR Bachelor’s degree plus 4 years of Manufacturing Operations experience
  • Experience in manufacturing, process development, or quality assurance within the biotech or pharmaceutical industry, with progressively increasing responsibility
  • Proficient in managing Change Controls and quality records (deviations, CAPAs, etc.) using systems like TrackWise, Vevaa, or similar
  • Possess project management and/or quality management skills, with demonstrated ability to coordinate cross-functional teams and deliver results on schedule
  • Demonstrate strong communication skills (written and verbal) in English, including technical writing and presentations
  • Adept at problem solving, critical thinking, and using Microsoft Office Tools and SAP (ERP) systems
  • Comfortable maintaining remote working relationships across a broad network
What’s a typical day as Specialist Manufacturing? You’ll be:
  • Supporting the execution of manufacturing and quality systems, including non-conformances, process validation, procedures, training, and new product introductions
  • Applying process, operational, and scientific expertise along with compliance knowledge to troubleshoot and resolve issues in manufacturing operations
  • Serving as the primary owner for production process support systems and assisting with process ownership responsibilities for complex systems
Kelly® Science & Clinical PR Offers!
  • Opportunity to work with a leading organization in the biotech/pharmaceutical industry
  • Gain hands-on experience supporting critical manufacturing and quality systems
  • Work in a collaborative, cross-functional environment with growth and learning opportunities
  • Career guides, information and tools to help you successfully position yourself throughout every stage of your career 
  • Access to more than 3,000 online training courses through our Kelly® Learning Center
  • Competitive pay rate with weekly direct deposit. Bi-Weekly pay by W-2. 
  • Vacations, Sick & Holidays paid*
  • Christmas bonus*
    • *Must comply with minimum established requirements to qualify.
Helping you discover what’s next in your career is what we’re all about, so let’s get to work.
Apply to be Specialist Manufacturing today!
Recruiter Lilly Abouomar 9395454792
#SETTPuertoRico
 
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.