... biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated ... Responsible for projects associate to component acceptance activities and inspections process.
... biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated ... Responsible for projects associate to component acceptance activities and inspections process.
... biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated ... Associate or Bachelor's (Preferred) in Human Resources, Business Administration, or a related field.
... biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated ... Associate or Bachelor's (Preferred) in Human Resources, Business Administration, or a related field.
... biotechnology, or medical device environments * Intermediate computer skills (Office 365 ... Ensure technicians follow proper calibration and testing procedures aligned with manufacturer ...
... biotechnology, or medical device environments * Intermediate computer skills (Office 365 ... Ensure technicians follow proper calibration and testing procedures aligned with manufacturer ...
... biotechnology, or medical device environments * Intermediate computer skills (Office 365 ... Ensure technicians follow proper calibration and testing procedures aligned with manufacturer ...
... biotechnology, or medical device environments * Intermediate computer skills (Office 365 ... Ensure technicians follow proper calibration and testing procedures aligned with manufacturer ...
... biotechnology, or medical device environments * Intermediate computer skills (Office 365 ... Ensure technicians follow proper calibration and testing procedures aligned with manufacturer ...
... biotechnology, or medical device environments * Intermediate computer skills (Office 365 ... Ensure technicians follow proper calibration and testing procedures aligned with manufacturer ...
Industrial Mechanic (Industria Regulada) - Vega Baja
Vega Baja, PR · On-site
$20.75 - $27/hr
... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, ... Study blueprints and manufacturers' manuals to determine correct installation and operation of ...
Industrial Mechanic (Industria Regulada) - Vega Baja
Vega Baja, PR · On-site
$20.75 - $27/hr
... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, ... Study blueprints and manufacturers' manuals to determine correct installation and operation of ...
Biotech Manufacturing Associate information
See Ponce, PR salary details
$11.99 - $13.87
5% of jobs
$13.87 - $15.75
17% of jobs
$15.97 is the 25th percentile. Wages below this are outliers.
$15.75 - $17.63
24% of jobs
The median wage is $18.02 / hr.
$17.63 - $19.51
18% of jobs
$19.51 - $21.39
9% of jobs
$21.73 is the 75th percentile. Wages above this are outliers.
$21.39 - $23.27
7% of jobs
$23.27 - $25.15
3% of jobs
$25.15 - $27.03
3% of jobs
$27.03 - $28.91
3% of jobs
$28.91 - $30.79
5% of jobs
$30.79 - $32.67
4% of jobs
$11
$20
$32
How much do biotech manufacturing associate jobs pay per hour?
As of Jul 28, 2026, the average hourly pay for biotech manufacturing associate in Ponce, PR is $20.38, according to ZipRecruiter salary data. Most workers in this role earn between $15.96 and $22.79 per hour, depending on experience, location, and employer.
What are Biotech Manufacturing Associates?
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 jobs can I get with an associate's degree in biotechnology?
Biotech Manufacturing Associates are common roles for those with an associate's degree in biotechnology, involving tasks such as preparing and operating laboratory equipment, following strict safety protocols, and documenting processes. Other positions include quality control technician, laboratory technician, and production operator, often requiring knowledge of GMP standards and familiarity with lab tools and procedures.
What does a biotech associate do?
A biotech manufacturing associate is responsible for performing tasks related to the production of biotechnological products, such as preparing equipment, following manufacturing protocols, and ensuring quality control. They often work in laboratory or cleanroom environments, using tools like bioreactors and adhering to safety and regulatory standards. Strong attention to detail and knowledge of GMP (Good Manufacturing Practice) are essential for this role.
What does a biotech manufacturing associate do?
A biotech manufacturing associate is responsible for producing, processing, and packaging biological products in a manufacturing environment. They operate equipment, follow strict safety and quality protocols, and document production activities to ensure compliance with regulatory standards. The role often requires attention to detail, knowledge of GMP practices, and the ability to work in a team setting.
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 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.
How much does a manufacturing associate make at KBI Biopharma?
A Biotech Manufacturing Associate at KBI Biopharma typically earns between $50,000 and $70,000 annually, depending on experience and location. The role involves working in a regulated environment, often requiring knowledge of GMP protocols and bioprocessing equipment.
What are the key skills and qualifications needed to thrive as a Biotech Manufacturing Associate, and why are they important?
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 cities near Ponce, PR are hiring for Biotech Manufacturing Associate jobs? Cities near Ponce, PR with the most Biotech Manufacturing Associate job openings:
Temporary
Posted 5 days ago
Job description
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
Qualifications:
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
Responsibilities:
- Ensures that suppliers deliver quality parts, materials, and services.
- Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness.
- Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur.
- Responsible for projects associate to component acceptance activities and inspections process.
- Implement and work with inspection plans
- Review measurement qualification method.
- Negotiation with suppliers to implement correct acceptance activities and inspections process.
- Supplier qualification
Qualifications:
- Bachelor's degree in Engineering.
- 3+ years of experience in Supplier Quality, Quality Engineering, or Manufacturing Quality.
- Experience in regulated industries such as Medical Devices, Pharmaceutical, or Biotechnology.
- Knowledge of GMP, ISO 13485, FDA regulations, and quality management systems.
- Experience conducting supplier audits and supplier qualification activities.
- Familiarity with CAPA, Root Cause Analysis, FMEA, Control Plans, and Statistical Sampling techniques.
- Experience supporting New Product Development (NPD) and product transfer activities.
- Strong problem-solving, analytical, and communication skills.
- Ability to work effectively with cross-functional teams and external suppliers.
- ASQ CQE, CSQP, Lead Auditor, or Six Sigma certification preferred.
- Proficiency in English, both written and verbal.
- First shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
About Quality Consulting Group
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