QRC Group, LLC

Process Engineer with experience in process validation among other related. Also experience with Protocols execution IQ/OQ/PQ Documentation and Validation activities. RequirementsBS Engineering5 years of experience in the Medical Devices industryKnowledgeable in Protocols execution IQ More...

Validation Specialist with experience in regulated industry validating/qualifying laboratory equipment manufacturing equipment processes utilities and facilities.Tasks:Execute complete validation cycleChange ControlEquipment qualification (manufacturing and laboratory)RequirementsBach More...

Validation Specialist with experience in aseptic areas. Knowledege and experience validating tanks and aseptic filling equipment. RequirementsBachelors degree in sciences and five years experience in related field. Bilingual (Spanish/English)Technical Writing Computer Literacy

Sr Manager Aseptic Process Engineering with experience in regulated industry. Will provide manufacturing engineering leadership and support to a diverse integrated supply chain by partnering with the extended Pharma Engineering function site engineering and other Pharma Operations pa More...

The Recruiter is responsible for sourcing attracting interviewing and supporting top talent to meet client s staffing needs while ensuring a positive candidate experience and alignment with business goals and metrics. As Payroll Assistant they are responsible for supporting the payr More...

Project Manager with experience on: Team working capabilities to serve and collaborate with crossfunctional groups Continuous improvement and productivity projects Metrics oversight Budget Management Critical thinkingSpecific responsibilities include but are not limited More...

Engineer with experience in Biotech companies (would be a plus) statistical analyses experience and drug substance manufacturing/technical support.RequirementsMaster s degree OR Bachelor s degree in Engineering & 2 years of Engineering experience(Preferred background: Chemical More...

Project Manager to lead and manage projects particularly in the development validation and FDA submission processes for pharmaceutical and medical device products.Responsibilities: Develop project timelines resource allocation plans and budgets ensuring timely and onbudget delivery.Co More...

Documentation Clerk with experience working in FDA regulated environment knowledge of cGMPs including Good Documentation Practices.RequirementsComputer literateAssociate Degree or High School Diploma and 1 year of experience in a GMP environment.Bilingual: English and Spanish

Process Development Sr Associate Scientist to:Conduct research into the structures and properties of materials such as metals polymers and ceramics to obtain information that could be used to develop new products or enhance existing ones.Determine ways to strengthen or combine materia More...

Specialist Quality Control with experience in the Pharmaceutical Industry Quality Control Laboratory Testing Project Management and Quality Processes (Microbiologist Chemist Biochemistry Molecular Sciences or Chemical Engineering). With knowledge in:Scientific Data AnalysisComputer Sy More...

Engineer with experience in regulated industry.Knowledge and experience in: Data AnalysisAseptic operation (filling and support)Engineering reliability elements and process excellence Maintenance systems and asset management Shift: 8am5pm OT based on business needs.RequirementsBachel More...

Engineer with experience in biotechnology or pharmaceutical industry. Duties:Work with Manufacturing to develop user.Supporting industrial process equipment and biotechnology manufacturing facilities. Develop project schedule of installation and qualification activities.Work directly More...

CSV Specialist to provide technical support to a pharmaceutical facility with experience in tag system preferably in packing areas. RequirementsBachelor in Science (Chemistry Engineering Microbiology Biochemistry) or related field and5 years of experience as CSV consultant in regulate More...

CSV Specialist to provide technical support to a pharmaceutical facility with experience in solid and semisolid manufacturing preferably in dispensing systems tablets capsules and granulation of active excipients.RequirementsBachelor in Science (Chemistry Engineering Microbiology Bioc More...

Process Development Scientist with knowledge in:Vision system technologies (Strong)Inspection/packaging Concepts Development and Execution of Processes/Equipment CharacterizationEstablish Testing StrategiesDesign / Development of Characterization ProtocolsTechnical Reports Development More...

Complaints Investigator with prior investigation experience in Parenteral or Solid Dosage. Duties: Investigate Complaints related to Manufacturing OperationsCoordinate investigationCollect data from available systems and/or data repositories Support impact evaluation of complaints fr More...

EHS Specialists with experience in Pharmaceutical or Medical devices industries. Responsible for planning implementing and enforcing an organization s Environmental Health and Safety (EHS) policies and procedures. To perform: Ensure that the company complies with all Occupational S More...

Process Development Scientist with experience in regulated industries. Technical Skills: Vision systems and Vision Tools (Cognex Systech Optel Keyence EISAI/BOSH/Syntengon Seidenader Brevetti MvTech) Analog and digital cameras technology Camera Systems illumination lenses and frame g More...

Specialist Tech Engineering with experience in regulated industries. Knowledge in Maximo data entry data sheets job plans and drawings. RequirementsBachelors Degree in Engineering and five years experience or related field. Engineering Experience Bilingual (English and Spanish)