Candidate Careers

Consultant, EtO Sterilization Validation Engineer / Sterilization SME, Medical Device Summary Our client, an innovative medical device company, has engaged GForce Life Sciences to provide an experienced EtO Sterilization Validation...

Consultant, Program Integration & Technical Oversight Lead, Construction   Summary  Our client, a global Fortune 500 medical device company, has engaged GForce to provide a Program Integration & Technical Oversight...

Senior Embedded Software Test Engineer 6-Month Contract Onsite – San Jose, CA Must be able to work on a W2 Summary Our client, a Fortune 500 Medical Device Company, has...

HEOR Consultant III 12-month Contract Remote- EST Hours Required Requirements Contribute to health economics projects by performing evidence synthesis, outcome research, and related analytical tasks under the direction of project...

Documentation Specialist 4-month Contract On-site in Scarborough, ME Must be able to work on a W2   Requirements Review and process change requests for new documents and revisions to existing documents. Process, organize, and maintain the Document Control System in accordance with applicable quality and regulatory guidelines. Review, edit, and approve or reject Quality System documents; ensure changes are appropriate, justified, and approved by required functional areas according to established procedures. Review documents for consistency with similar or related product specifications and labeling. Secure and control access of documentation as required by established procedures. Communicate and coordinate documentation approvals with other sites. Participate on cross-functional project teams. Follow EHS rules and procedures; report EHS incidents and/or unsafe acts and conditions promptly to supervision; forward opportunities to improve the EHS program to supervision. Implement and maintain the effectiveness of the Quality System. Ensure accuracy of documentation, as product quality is directly linked to associated documentation. Perform other duties and responsibilities as assigned. Qualifications Minimum of 2 or more years of relevant work experience or exposure within a regulated environment. Associate’s Degree or equivalent combination of education and work experience; Bachelor’s Degree preferred and may account for experience requirement. Ability to clearly, concisely, and accurately convey communications. Ability to influence and provide leadership related to documentation requirements. Ability to form and develop interpersonal, professional relationships. Display socially and professionally appropriate behavior. Ability to work independently and in groups. Demonstrated initiative and problem-solving skills. Strong critical-thinking skills. Ability and aptitude to use various types of databases and other computer software. Ability to prioritize tasks effectively. Strong organizational skills and ability to manage projects....

Consultant, Regulatory & Quality Lead, Medical Devices   Summary  Our client, a growing medical device firm, has engaged GForce to provide a Regulatory & Quality Lead to serve as the...

Sourcing Execution Manager IV 12-month Contract Remote – EST hours Must be able to work on a W2 Summary Our client, a Fortune 500 Pharmaceutical Company, has engaged GForce Life...

Quality Associate 12- month Contract Remote – EST Hours Description Our client, a Fortune 500 Pharmaceutical Company, has engaged GForce Life Sciences to provide a Quality Associate to support Global...

Internal Communications and Business Manager 18- Month Contract Remote- EST Hours Must be able to work a W-2 Pay Rate: starting at $50/hr Requirements Develop and implement internal communication strategies...

Data Analyst 12-month Contract Remote- EST Hours   Description The Data Analyst will be responsible for translating complex analytics into clear, actionable insights to support brand strategy and executive decision-making....

Regulatory Affairs Associate 6-month Contract Onsite – Sylmar, CA Must be able to work on a W2 Requirements Prepare, author, and submit U.S. FDA PMA supplements, including: 30-Day Notices Real-Time...

Quality Control Technician 5-month Contract Onsite – Scarborough, ME Must be able to work on a W2 Summary Our client, a Fortune 500 Medical Device Company, has engaged GForce Life...