Empleos en Carolina pr pr
Quality Compliance Specialist
Share Tech GroupCarolina, PR
Steward
Sonesta HotelsRoyal Sonesta San Juan, PR
Personal de Mantenimiento $11.50
Prime Janitorial ServiceCarolina, PR, PR
Pharmacy Intern Year
WalgreensCAROLINA, PR- Oferta promocionada
U.S. Customs and Border Protection Officer
U.S. Customs and Border ProtectionCarolina, PR, United States
EHS Specialist
Flexible & Integrated Technical Services, LLCCarolina, PR, PR
Supervisor / Manager Part-Time
Claire'sCarolina, PR
Warehouse Agent
Alliance Ground InternationalCarolina, PR
Driver - Food Service / Vending Product Delivery (PepsiCo) $16-$35 / hr
PepsiCoCarolina, PR, United States
Asociado de Mantenimiento
Crunch - PonceCarolina, PR
Contable
Kelly ServicesCarolina, PR, United States
Esthetician
Trilogy Spa HoldingsCarolina, PR
Casino Table Games Manager
HighgateCarolina, PR
Aircraft Refueling Operator
World Fuel ServicesCAROLINA, PR
Bartender / Texas Roadhouse
Texas RoadhouseCarolina, PR
PetSmart is hiring : Retail Sales Associate Part Time (PR) in Carolina
PetSmartCarolina, PR, United States
Se necesitan conductores en San Juan
LyftCarolina, PR, United States
Licensed Electrician (Perito Electricista)
Mentor Technical GroupCarolina, PR
PetSmart is hiring : Retail Store Manager (PR) in Carolina
MediabistroCarolina, PR, United StatesQuality Compliance Specialist
Share Tech GroupCarolina, PR- Quick Apply
We are seeking a Quality Compliance Specialist with strong expertise in GMP regulations and proven experience in Oral Solid Dosage (OSD) operations.
The ideal candidate will contribute to ensuring compliance, supporting qualification strategies, and applying best practices in facility and process design aligned with industry standards.
Key Responsibilities : Ensure compliance with current Good Manufacturing Practices (cGMP) in all quality systems and manufacturing operations.
Support and / or lead qualification strategies for equipment, utilities, and facilities related to OSD.
Participate in cross-functional teams during the design and construction of new or modified OSD facilities.
Provide quality oversight for manufacturing, validation, cleaning, and packaging of oral solid dosage forms.
Review and approve documentation such as SOPs, protocols, deviations, and CAPAs.
Conduct risk assessments and gap analyses to drive continuous improvement.
Collaborate with Engineering and Validation teams to ensure best practices are applied in OSD facility design.
Requirements : Bachelor’s degree in Pharmacy, Chemistry, Engineering, or Life Sciences.
5+ years of experience in a Quality role within the Pharmaceutical industry, with strong focus on OSD manufacturing.
In-depth knowledge of FDA and international GMP regulations.
Experience in qualification / validation strategies (IQ / OQ / PQ).
Familiarity with ISPE, ASTM, and ICH guidelines.
Strong analytical, communication, and problem-solving skills.
Bilingual preferred : English & Spanish.
Preferred Qualifications : Experience with design and startup of OSD manufacturing areas.
Certification in Lean, Six Sigma, or Quality Assurance.
Experience interacting with regulatory agencies.
Candidate should be able to commute to site since relocation is not available. "Drug Free Workplace Policy : In accordance with our commitment to maintaining a safe and productive work environment, all applicants for employment with our company are required to affirm their commitment to a drug-free workplace and consent to pre-employment drug testing as a condition of employment." Share Tech Group is committed to being an equal opportunity employer, fostering a diverse and inclusive workplace where all individuals are treated with respect and provided with equal opportunities for employment and advancement.
Powered by JazzHR