PR · On-site
... Biotech and manufacturing experience SUMMARY With minimal supervision, support the execution of ... Associates + 8 years of Manufacturing Operations experience OR -High school/GED + 10 years of ...
Quick apply
PR · On-site
... Biotech and manufacturing experience SUMMARY With minimal supervision, support the execution of ... Associates + 8 years of Manufacturing Operations experience OR -High school/GED + 10 years of ...
Specialist Manufacturing
Juncos, PR · On-site
Associate degree + 8 years of Manufacturing Operations experience, OR * High school/GED + 10 years ... Hands‑on experience in manufacturing operations within biotech, pharmaceutical, or other ...
Quick apply
Specialist Manufacturing
Juncos, PR · On-site
Associate degree + 8 years of Manufacturing Operations experience, OR * High school/GED + 10 years ... Hands‑on experience in manufacturing operations within biotech, pharmaceutical, or other ...
Specialist Manufacturing
Juncos, PR · On-site
... or Associate's degree and 10 years of Manufacturing Operations experience or High school diploma ... Biotech and manufacturing experience Skills: * Detailed technical understanding of bioprocessing ...
New
Quick apply
Specialist Manufacturing
Juncos, PR · On-site
... or Associate's degree and 10 years of Manufacturing Operations experience or High school diploma ... Biotech and manufacturing experience Skills: * Detailed technical understanding of bioprocessing ...
New
Specialist Manufacturing
Juncos, PR · On-site
... environment (biotech, pharmaceutical, or similar). Technical Knowledge - Familiarity with ... Associates + 8 years of Manufacturing Operations experience OR -High school/GED + 10 years of ...
Specialist Manufacturing
Juncos, PR · On-site
... environment (biotech, pharmaceutical, or similar). Technical Knowledge - Familiarity with ... Associates + 8 years of Manufacturing Operations experience OR -High school/GED + 10 years of ...
... environment (biotech, pharmaceutical, or similar). Technical Knowledge - Familiarity with ... Associates + 8 years of Manufacturing Operations experience OR -High school/GED + 10 years of ...
Quick apply
... environment (biotech, pharmaceutical, or similar). Technical Knowledge - Familiarity with ... Associates + 8 years of Manufacturing Operations experience OR -High school/GED + 10 years of ...
Specialist Manufacturing
Juncos, PR · On-site
... or Associate's degree and 10 years of Manufacturing Operations experience or High school diploma ... environment (biotech, pharmaceutical, or similar). * Technical Knowledge - Familiarity with ...
New
Quick apply
Specialist Manufacturing
Juncos, PR · On-site
... or Associate's degree and 10 years of Manufacturing Operations experience or High school diploma ... environment (biotech, pharmaceutical, or similar). * Technical Knowledge - Familiarity with ...
New
Specialist Manufacturing
Medical
Dental
Vision
... or Associate's degree and 10 years of Manufacturing Operations experience or High school diploma ... Experience in biotechnology pharmaceutical process support, especially on Drug Substance processes ...
Specialist Manufacturing
Medical
Dental
Vision
... or Associate's degree and 10 years of Manufacturing Operations experience or High school diploma ... Experience in biotechnology pharmaceutical process support, especially on Drug Substance processes ...
Senior Engineer 35627
$101K - $139K/yr
Pharmaceutical or biotechnology manufacturing environments. * Knowledge of regulated manufacturing ... Coordinate and review the work of engineers, associates, technicians, and project team members.
Quick apply
Senior Engineer 35627
$101K - $139K/yr
Pharmaceutical or biotechnology manufacturing environments. * Knowledge of regulated manufacturing ... Coordinate and review the work of engineers, associates, technicians, and project team members.
Sr Data Scientist
Juncos, PR · On-site
$110 - $150/hr
... Associates + 8 years of data science, business, statistics, data mining, applied mathematics ... Biotechnology, Manufacturing Engineering, or a related technical discipline) #J-18808-Ljbffr
Sr Data Scientist
Juncos, PR · On-site
$110 - $150/hr
... Associates + 8 years of data science, business, statistics, data mining, applied mathematics ... Biotechnology, Manufacturing Engineering, or a related technical discipline) #J-18808-Ljbffr
Sr Engineer
Juncos, PR · On-site
$101K - $139K/yr
Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians ... biotechnology manufacturing environment. Experience should include: * Preparation, review, and ...
New
Quick apply
Sr Engineer
Juncos, PR · On-site
$101K - $139K/yr
Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians ... biotechnology manufacturing environment. Experience should include: * Preparation, review, and ...
New
PR · On-site
$102K - $140K/yr
Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians ... biotechnology manufacturing environment. Experience should include: * Preparation, review, and ...
Quick apply
PR · On-site
$102K - $140K/yr
Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians ... biotechnology manufacturing environment. Experience should include: * Preparation, review, and ...
Scheduler / Planning Engineer
Humacao, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Humacao, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Gurabo, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Gurabo, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Quick apply
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Quick apply
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Humacao, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Humacao, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Juncos, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Juncos, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Quick apply
PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Gurabo, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Gurabo, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Juncos, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Scheduler / Planning Engineer
Juncos, PR · On-site
... biotechnology manufacturing environments by developing, maintaining, and coordinating project ... Associate's or Bachelor's degree in Project Management, Construction Management, Engineering ...
Biotech Manufacturing Associate information
What is a biotech manufacturing associate?
Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.
What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?
To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.
What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?
Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.
What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?
| Aspect | Biotech Manufacturing Associate | Laboratory Technician |
|---|---|---|
| Credentials | High school diploma or equivalent; some roles may require associate degree | High school diploma or equivalent; some roles may require associate degree or certification |
| Work Environment | Manufacturing floor, production lines, cleanrooms | Laboratories, research facilities, testing environments |
| Industry Usage | Biotech manufacturing, pharmaceutical production | Research labs, quality control, testing labs |
While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.
What job categories do people searching Biotech Manufacturing Associate jobs in Puerto Rico look for?
The top searched job categories for Biotech Manufacturing Associate jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Biotech Manufacturing Associate jobs?
Cities in Puerto Rico with the most Biotech Manufacturing Associate job openings:
Job description
We are seeking a visionary Specialist Manufacturing professional to drive production excellence at the intersection of precision engineering and automation. In this role, you will optimize advanced manufacturing processes, implement cutting-edge Industry 4.0 technologies, and scale production lines to deliver next-generation products that shape our industry
What attributes (i.e. - preferred qualifications) would make this candidate stand out?
Bachelor's degree in engineering is a plus
Deviations management
Deviation assessments
Track wise
Biotech and manufacturing experience
SUMMARY
With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations. May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.
FUNCTIONS
Applied Process Expertise
1. Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
2. Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.
3. Provide troubleshooting support.
4. Assist in generation of training materials and may assist in providing training on scientific or technical aspects of the process.
Process Monitoring
1. Support establishment of process monitoring parameters and control limits. Collect process-monitoring data and support the assessment of deviations.
2. Provide support of timely execution of the process monitoring quarterly reports.
Non-Conformance and CAPA
1. Ensure that all Non-conformances are triaged within the established goal.
2. Responsible for authoring investigation reports.
3. Responsible for execution of corrective actions.
4. Responsible for managing NC/CAPA closure within established goal.
5. Monitor and communicate incidents trends.
6. Review equipment/system Root Cause Analysis investigations and support trend evaluations.
Process Validation
1. Assist with generation of process validation protocols and reports.
2. Assist with the execution of the process validation.
3. Support collection and analysis of process validation data.
Regulatory
1. May participate in regulatory inspections, New Product Introductions, and Process or Equipment Modifications:
1. Participate in the NPI process to assess requirements for documentation, materials, training, and equipment modifications.
2. Assess, prioritize, justify, and provide implementation and project management support for process or equipment modification projects.
Change Control
1. Assist manufacturing change owner on CCRB packages impacting the process.
Projects and Initiatives
1. Participate on the assessment or implementation of special projects or initiatives.
** Other functions may be assigned.
EDUCATION/LICENSES
-Doctorate OR Master's + 2 years of Manufacturing Operations experience OR -Bachelors + 4 years of Manufacturing Operations experience OR -Associates + 8 years of Manufacturing Operations experience OR -High school/GED + 10 years of Manufacturing Operations experience.
COMPETENCIES/SKILLS
- Detailed technical understanding of bioprocessing unit operations.
- Skilled in performance of GMP production operations.
- Regulatory knowledge and interactions.
- Participate and help lead cross-functional teams.
- Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.
- Organizational, technical writing and presentation skills.
- Basic project management skills.
- Basic knowledge of control charting.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*
What attributes (i.e. - preferred qualifications) would make this candidate stand out?
Bachelor's degree in engineering is a plus
Deviations management
Deviation assessments
Track wise
Biotech and manufacturing experience
SUMMARY
With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations. May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.
FUNCTIONS
Applied Process Expertise
1. Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
2. Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.
3. Provide troubleshooting support.
4. Assist in generation of training materials and may assist in providing training on scientific or technical aspects of the process.
Process Monitoring
1. Support establishment of process monitoring parameters and control limits. Collect process-monitoring data and support the assessment of deviations.
2. Provide support of timely execution of the process monitoring quarterly reports.
Non-Conformance and CAPA
1. Ensure that all Non-conformances are triaged within the established goal.
2. Responsible for authoring investigation reports.
3. Responsible for execution of corrective actions.
4. Responsible for managing NC/CAPA closure within established goal.
5. Monitor and communicate incidents trends.
6. Review equipment/system Root Cause Analysis investigations and support trend evaluations.
Process Validation
1. Assist with generation of process validation protocols and reports.
2. Assist with the execution of the process validation.
3. Support collection and analysis of process validation data.
Regulatory
1. May participate in regulatory inspections, New Product Introductions, and Process or Equipment Modifications:
1. Participate in the NPI process to assess requirements for documentation, materials, training, and equipment modifications.
2. Assess, prioritize, justify, and provide implementation and project management support for process or equipment modification projects.
Change Control
1. Assist manufacturing change owner on CCRB packages impacting the process.
Projects and Initiatives
1. Participate on the assessment or implementation of special projects or initiatives.
** Other functions may be assigned.
EDUCATION/LICENSES
-Doctorate OR Master's + 2 years of Manufacturing Operations experience OR -Bachelors + 4 years of Manufacturing Operations experience OR -Associates + 8 years of Manufacturing Operations experience OR -High school/GED + 10 years of Manufacturing Operations experience.
COMPETENCIES/SKILLS
- Detailed technical understanding of bioprocessing unit operations.
- Skilled in performance of GMP production operations.
- Regulatory knowledge and interactions.
- Participate and help lead cross-functional teams.
- Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.
- Organizational, technical writing and presentation skills.
- Basic project management skills.
- Basic knowledge of control charting.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*
About Weil Group
Sourced by ZipRecruiter
Company size
1 - 10 Employees
Headquarters location
Richmond, VA, US
Year founded
2011