GMP Data Reviewers, Chemists, Metrology, LabWare, CPU Validation

Quality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in...

Quality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in...

Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Validation Engineer. This position, in the Manufacturing and Formulations Services department, requires a Bachelor’s degree or higher in a scientific or engineering discipline with either 3...

Qualifications: Associate’s degree or higher preferred with 1-2 years of experience or 4-5 years working experience in metrology/information technology / customer service or other relevant field. Experience working in a GMP environment and maintaining laboratory equipment. Highly organized, strong communication skills. Capable of working independently....

Company DescriptionSonsoft , Inc. is a USA based corporation duly organized under the laws of the Commonwealth of Georgia. Sonsoft Inc. is growing at a steady pace specializing in the fields of Software Development, Software Consultancy and Information Technology Enabled Services.Job DescriptionAt least 9 years of experience in Business Process Consulting,...

100% onsite Responsibilities:Review and approve vendor-executed calibration, maintenance, repair, and performance verification work.Prepare documentation for Quality Assurance approval prior to work execution.Monitor schedules to ensure timely completion of calibration, performance verification testing, and maintenance services.Ensure calibration testing on...

Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of QA Associate – Report Generation. The candidate will be responsible for review and approval of reports generated from laboratory data, such as certificate of analysis and stability study...

Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Validation Engineer. This position, in the Manufacturing and Formulations Services department, requires a Bachelor’s degree or higher in a scientific or engineering discipline with either 3...

Job DescriptionJob DescriptionBenefits:401(k)Competitive salaryDental insuranceHealth insurance Seeking qualified Chemist w/Masters or foreign equiv degree in Pharmacy or Science or Chemistry & 6 months of work experience to Perform routine manufacturing batch production record review in support of product batch release in accordance with specifications and...

Our client is a global, research-driven pharmaceutical focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a Validation Engineer to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference! Shift : M-F 1st shift Type : 7...

What You'll Do o Commissioning Forms o C/Q/V Protocols and Summary Reports o Standard Operating Procedures o Impact Assessments o Specifications (URS/FRS/DDS) o FATS/SATs  Perform field/site activities including, but not limited to, the following: o Attend and witness FATs and SATs o Execution of commissioning forms and witnessing vendor start-up and...

Title: Principal Engineer Location: New Albany, OH Duration: 12 months The Engineer will support the development and implementation of technical solutions for a variety of engineering initiatives supporting the FDP commercial GMP operations. The position is a key role in the Process Development group and the candidate must manage and/or apply extensive...

Not For C2C Candidates Please do not apply even not enquire Job Title: CQV Validation Engineer Location: Countrywide USA Contract Duration: 12+ months Pay: Negotiable on w2 without any benefits Responsibilities: Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and...

Title: Principal EngineerLocation: New Albany, OHDuration: 12 monthsThe Engineer will support the development and implementation of technical solutions for a variety of engineering initiatives supporting the FDP commercial GMP operations. The position is a key role in the Process Development group and the candidate must manage and/or apply extensive...

Title: Principal EngineerLocation: New Albany, OHDuration: 12 monthsThe Engineer will support the development and implementation of technical solutions for a variety of engineering initiatives supporting the FDP commercial GMP operations. The position is a key role in the Process Development group and the candidate must manage and/or apply extensive...

Title: Principal EngineerLocation: New Albany, OHDuration: 12 monthsThe Engineer will support the development and implementation of technical solutions for a variety of engineering initiatives supporting the FDP commercial GMP operations. The position is a key role in the Process Development group and the candidate must manage and/or apply extensive...

Not For C2C Candidates Please do not apply even not enquire Job Title: CQV Validation Engineer Location: Countrywide USA Contract Duration: 12+ months Pay: Negotiable on w2 without any benefits Responsibilities: Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and...

Not For C2C Candidates Please do not apply even not enquire Job Title: CQV Validation Engineer Location: Countrywide USAContract Duration: 12+ monthsPay: Negotiable on w2 without any benefitsResponsibilities:Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and...

Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of QA Associate – Report Generation. The candidate will be responsible for review and approval of reports generated from laboratory data, such as certificate of analysis and stability study...

Senior Validation Engineer Are you a validation expert looking for a new, dynamic environment? I am partnering with a rapidly growing full service CDMO who are specialised within sterile product development, manufacturing and packaging, and am working with the leadership team to help appoint a number of new hires. For this specific hire, we are seeking and...