We are seeking a Validation Specialist for a contract opportunity supporting laboratory equipment validation in a regulated pharmaceutical manufacturing environment in Jayuya, Puerto Rico. This role is ideal for an early-career validation professional with hands-on experience executing qualification protocols and documenting results in compliance with cGMP and Good Documentation Practices. Required Qualifications and Skills
The Validation Specialist will work on-site to help ensure laboratory instruments and equipment are properly qualified, documented, and ready for use. This is a strong opportunity to gain valuable pharmaceutical validation experience in a structured, compliance-focused setting with supportive project leadership, collaborative teamwork, and exposure to critical equipment qualification activities.
Key Responsibilities
- Execute validation and qualification activities for laboratory equipment in accordance with approved protocols, SOPs, cGMP requirements, and regulatory standards.
- Support the development, review, execution, and completion of validation protocols and related documentation.
- Perform IQ, OQ, and PQ activities for laboratory instruments and equipment as applicable.
- Document validation results accurately, including supporting evidence, traceability, discrepancies, and deviations.
- Collaborate with Quality, Laboratory, Engineering, Manufacturing, and other teams to support equipment readiness and validation deliverables.
- Participate in project meetings, provide status updates, and manage assigned tasks to meet project timelines and quality expectations.
Compensation and Benefits
- Pay Rate: $25.00 to $45.00 per hour.
- Job Type: Contract/Temporary.
- Project Duration: Approximately 1 year.
- Location: Jayuya, Puerto Rico.
- Work Arrangement: On-site.
- Bachelor’s degree in Chemistry, Chemical Engineering, or a closely related scientific or engineering discipline.
- Minimum of 1 year of hands-on experience in validation or qualification of laboratory equipment, preferably in pharmaceutical, biotechnology, medical device, or another regulated industry.
- Experience executing validation protocols for laboratory instruments and equipment.
- Basic knowledge of equipment qualification concepts, including IQ, OQ, and PQ.
- Knowledge of cGMP, Good Documentation Practices, SOPs, and validation documentation requirements.
- Strong attention to detail and ability to work accurately in a regulated environment.
- Ability to manage multiple assignments, meet timelines, and maintain quality expectations.
- Strong organizational, analytical, and problem-solving skills.
- Ability to work independently and collaboratively with cross-functional teams.
- Proficiency with Microsoft Office applications, including Excel, Word, and PowerPoint.
- Bilingual in English and Spanish, written and verbal.
- Ability to work on-site in a pharmaceutical manufacturing and laboratory environment.
- Ability to stand for extended periods, climb ladders or steps when required, and lift items weighing up to 25 lbs.
- Ability to wear appropriate gowning and PPE in laboratory and manufacturing areas as required by GMP and OSHA requirements.
- Flexibility to work extended shifts depending on project requirements.
Preferred Qualifications
- Experience supporting validation activities within pharmaceutical manufacturing or laboratory operations.
- Familiarity with equipment commissioning and readiness activities.
- Experience supporting discrepancy resolution, investigations, deviations, or corrective actions related to validation execution.
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