Location: all cities,NY, USA
Job Title: Validation engineer
Location: Open to Relocation (Anywhere in the U.S.)
Job Type: Contract (W2)
Duration: 6-12 months
Experience: Minimum 1 year in the pharmaceutical industry
Job Description:
We are looking for a Validation Engineer with experience in the pharmaceutical industry. The ideal candidate should be willing to relocate for a contract-based role and have a solid understanding of validation processes for equipment and systems used in manufacturing. This position is ideal for candidates with at least one year of experience in the industry who are willing to relocate across the U.S. for exciting project-based opportunities.
Responsibilities:
Conduct validation activities for manufacturing equipment, cleaning processes, and computerized systems.
Develop and execute validation protocols (IQ/OQ/PQ) for new and existing equipment.
Collaborate with cross-functional teams to ensure equipment and processes meet industry standards and regulations.
Document validation results, deviations, and corrective actions.
Perform risk assessments and create validation documentation according to GMP requirements.
Ensure compliance with FDA, ISO, and other regulatory standards.
Qualifications:
Bachelor's degree in Engineering, Life Sciences, or related field.
At least 1 year of experience in validation within the pharmaceutical or biotech industry.
Knowledge of GMP, GAMP, and validation guidelines.
Quality Control Analyst (Contract, W2)
Location: Open to Relocation (Anywhere in the U.S.)
Job Type: Contract (W2)
Duration: 6-9 months
Experience: Minimum 1 year in quality control within the pharmaceutical industry
Job Description:
Seeking a detail-oriented Quality Control Analyst to join our team on a contract basis. The position requires a candidate with at least 1 year of experience in a QC laboratory who is open to relocating for the role.
Responsibilities:
Perform routine testing of raw materials, intermediates, and finished products using HPLC, GC, and other analytical techniques.
Conduct stability testing and prepare reports for regulatory submissions.
Maintain laboratory documentation in accordance with GMP and GLP requirements.
Ensure proper calibration and maintenance of laboratory equipment.
Participate in laboratory investigations and assist in root cause analysis.
Collaborate with the Quality Assurance team to ensure data integrity and compliance.
Qualifications:
Bachelor's degree in Chemistry, Biochemistry, or related field.
1+ years of experience in a quality control environment within the pharmaceutical industry.
Experience with analytical techniques such as HPLC, GC, FTIR, and UV-Vis.