Compliance Engineer | Pharmaceutical | C&Q

Job DescriptionJob DescriptionLocation: On Site Industry: Pharmaceutical Manufacturing – Solid Dosage Position Type: ContractWe are seeking a motivated and detail-oriented Compliance Engineer to support projects and operations within a GMP-regulated pharmaceutical manufacturing environment. This role will focus on ensuring compliance, supporting C&Q-related activities, and partnering with cross-functional teams to maintain quality standards and operational excellence.The ideal candidate will bring experience in pharmaceutical manufacturing environments and enjoy working in collaborative, fast-paced settings that support engineering and manufacturing initiatives.Main ResponsibilitiesSupport compliance activities related to pharmaceutical engineering and C&Q projects.Partner with Project Execution and Engineering teams to support investigations and follow-up activities when needed.Assist with CAPA-related actions and support timely completion of quality initiatives.Monitor compliance-related metrics and help track completion of key quality activities.Review and support GMP documentation to ensure quality and compliance standards are met.Participate in change control, documentation review, and quality system activities.Support onboarding activities and coordinate documentation for new team members.Collaborate with Quality, Manufacturing, Engineering, and Validation teams.Support audit readiness and inspection preparation efforts.Assist with continuous improvement initiatives and process enhancement activities.Maintain accurate documentation and ensure compliance with internal procedures.General RequirementsKnowledge of GMP regulations and pharmaceutical compliance practices.Familiarity with Commissioning & Qualification (C&Q) processes and validation activities.Understanding of quality systems, documentation practices, CAPA, and change management.Strong organizational and communication skills.Ability to work independently and within cross-functional teams.Strong attention to detail and problem-solving mindset.Proficiency with Microsoft Office and electronic documentation systems.Experience with documentation platforms such as Kneat or similar systems is a plus.EducationBachelor’s degree in Engineering (Chemical, Mechanical, Industrial, Biomedical, Electrical, or related field)Life Sciences or related technical disciplineEquivalent experience in pharmaceutical environments may be considered.ExperienceMinimum 3+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments.Experience supporting compliance, quality, engineering, validation, or C&Q-related activities.Previous experience in pharmaceutical manufacturing environments required.Experience in Solid Dosage manufacturing is preferred.Experience with GMP documentation, CAPA, investigations, and quality systems is a plus.Experience supporting manufacturing operations and cross-functional project teams preferred.Physical RequirementsAbility to work in office and manufacturing environments.Ability to walk production areas and support field activities.May require prolonged periods sitting, standing, and computer use.Ability to occasionally lift up to 25 lbs.Ability to wear required PPE and cleanroom attire as needed.