Pharma QA Training Specialist – Onsite PR, Growth & Benefits

Kelly Services

Gurabo (PR)

On-site

USD 32,000 - 40,000

Full time

7 days ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Weekly pay
Paid vacations, sick days, and keephol
Christmas bonus
Benefits

Job summary

Kelly Life Science is seeking a QA Training Specialist to join our onsite team in Gurabo, PR. You will develop and deliver QA training programs, ensuring compliance with cGMPs and producing clear technical documentation.

Fluency in English and Spanish is required, with collaboration across departments in a fast-paced pharmaceutical setting. The role offers full-time hours in a standard administrative schedule with competitive benefits and career development opportunities within our network of

Qualifications

  • Bachelor’s degree in Natural Science or related field (required)
  • Minimum 2 years of experience in a similar position within the pharmaceutical industry
  • Experience in training and curricula development; ability to develop new training programs
  • Knowledge of cGMPs (current Good Manufacturing Practices), compliance, and technical writing
  • Strong computer and software skills
  • Excellent verbal and written communication skills in English and Spanish (bilingual)
  • Experience with compliance aspects preferred

Responsibilities

  • Develop and deliver training programs and curricula for QA and compliance.
  • Support the organization with training initiatives and program development.

Skills

Training & curricula development
Bilingual English/Spanish
Verbal & written communication
Computer skills

Education

Bachelor's degree in Natural Science or related field

Job description

Kelly Life Science is seeking a QA Training Specialist to join our onsite team in Gurabo, PR. You will develop and deliver QA training programs, ensuring compliance with cGMPs and producing clear technical documentation.

Fluency in English and Spanish is required, with collaboration across departments in a fast-paced pharmaceutical setting. The role offers full-time hours in a standard administrative schedule with competitive benefits and career development opportunities within our network of

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Onsite QA Training Specialist - GMP & Compliance Leader
Onsite QA Training Specialist - GMP & Compliance Leader

Mykelly • Gurabo (PR)

On-site
USD 32,000 - 40,000
Weekly pay
Benefits package
Onsite in Gurabo
QA Training Specialist
QA Training Specialist

Mykelly • Gurabo (PR)

On-site
USD 32,000 - 40,000
Weekly pay
Benefits package
Onsite in Gurabo
Quality Assurance Analyst II — On-Site Pharma
Quality Assurance Analyst II — On-Site Pharma

Medial Group • Gurabo (PR)

On-site
USD 60,000 - 80,000
Senior QA Specialist – GMP Biotech (Onsite)
Senior QA Specialist – GMP Biotech (Onsite)

Artech-Information-Systems-L.l.c. • Barceloneta (PR)

On-site
USD 50,000 - 57,000
Biopharma QA Specialist - Compliance & Validation Leader
Biopharma QA Specialist - Compliance & Validation Leader

ProQuality Network • Juncos (PR)

Hybrid
USD 70,000 - 110,000
Pharma QA Investigator — CAPA & Compliance Expert
Pharma QA Investigator — CAPA & Compliance Expert

Legal Project Management Partners • Arecibo (PR)

On-site
USD 65,000 - 90,000
Senior QA Specialist — cGMP & Compliance
Senior QA Specialist — cGMP & Compliance

Echo-Consulting-Group • Puerto Rico

On-site
USD 90,000 - 120,000
Biotech QA Specialist - GMP, CAPA & Change Control
Biotech QA Specialist - GMP, CAPA & Change Control

Biopharma-Consulting-Jad-Group • Juncos (PR)

On-site
USD 45,000 - 67,000
Senior QA Associate - Drug Product Compliance
Senior QA Associate - Drug Product Compliance

Kelly Services • Juncos (PR)

On-site
USD 41,000 - 47,000
medical
dental
vision
+12
QA Specialist 35563
QA Specialist 35563

ProQuality Network • Juncos (PR)

On-site
USD 70,000 - 110,000