QA Specialist

SupportFinity™; Deerfield Beach (FL); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Competitive compensation package

Modern working environment

Opportunities for personal and professional development

Job summary

A leading pharmaceutical company is seeking a QA Specialist in Deerfield Beach, Florida. The role involves overseeing GMP operations, reviewing batch records, and ensuring compliance with cGMP standards. Candidates should have a BS in Engineering, Biology, or a related field, along with a minimum of 4 years of experience in quality assurance within GMP environments. Competitive compensation and a dynamic work environment are offered. Join a growing team committed to innovation and excellence.

Qualifications

• Minimum of 4 years experience in Quality with Pharma/Medical Device GMP.
• Knowledge of FDA, EMA, JP regulations.
• Experience with internal/external audits.

Responsibilities

• Review and approve Production Batch Records and Testing Results.
• Maintain QA presence on the manufacturing floor.
• Support Audit Team during internal and external audits.

Skills

Quality assurance experience

Technical writing

Regulatory compliance knowledge

Problem-solving

Communication skills

Education

BS in Engineering, Biology, or related technical degree

Job description

SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self‑injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues.

Job Overview

QA Specialist provides oversight of GMP operations to ensure that products are manufactured according to cGMP requirements and fit for their intended use. Maintains data collected from the manufacturing process, generates, and updates procedures and ensures Batch Records comply with established policies and procedures.

Main Responsibilities

• Review and Approve Production Batch Records and Testing Results to ensure they are complete, accurate and documented according to established procedures.
• Prepare CoC and CoAs.
• Maintain QA manufacturing floor presence in support of manufacturing operations and provide oversight over process‑related decisions.
• Review and approve Quality Work Instructions (QWIs), Technical and Product Specifications, Sampling instructions and Test Methods.
• Provide oversight to Risk Management programs, procedures and documentation for Development and Process Validation activities.
• Review and approve Test Method Development, Validation and Transfer activities in support of the Analytical Sciences department.
• Review and approve Stability Studies protocols and reports.
• Support the investigation process for Non‑Conformances and ensure completion of related corrective and preventive actions.
• Support the Audit Team during external and internal audits.
• Provide support to the program management office with the review and approval of the design transfer package documentation.
• Provide Quality support throughout the product lifecycle to include the review of Annual product reviews, Product Process Monitoring activities and Continuous Improvement initiatives.

Skills And Qualification

• Preferred BS in Engineering, Biology, or other technical related degree
• A minimum of 4 years of experience in Quality with Pharmaceutical and/or Medical Device based GMP manufacturing operations.
• Proficient skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities.
• Demonstrate proficient ability to evaluate and apply compliance requirements/guidelines to complex situations.
• Knowledge of regulations and practices pertaining to pharmaceutical/medical device products in area of responsibility.
• Ability to interact with regulatory agencies and knowledge of FDA, EMA, JP and other regulations.
• Knowledge of Good Manufacturing Practices & Good Documentation Practices.
• Able to communicate effectively and work within cross‑functional teams.
• Excellent oral and written communication skills with strong technical writing experience required.
• Experience in internal / external audits, identify findings, drive resolution, and provide closure report.
• Proficient skills in solving complex problems and ability to bring issues to resolution.
• Experience working globally with diverse teams and cultures.

We Offer

• Competitive compensation package
• Modern working environment with state‑of‑the‑art facilities and technologies
• Challenging assignments in a fast growing and innovative industry
• Position in a dynamic, international team of highly skilled professionals
• Various opportunities for personal and professional development within a global organization

Please note that SHL is a drug free employer. This offer of employment is contingent upon your successful completion of various pre‑employment screenings, including, but not limited to, a drug test, employment verification, reference checks, and a criminal background check.

For more information on SHL Medical, please visit: shl‑medical.com