21-40 of 95 results
Sort By


We are looking for an Associate Director of Production to be responsible for overall manufacturing and packaging at a Pharmaceuticals facility. Major responsibilities include building teams, qualification of equipment, setting up plant systems and processes, site transfer of manufacturing processes, media fills, maintaining aseptic manufacturing areas and manufacturing of exhibit and commercial batches. The Associate Director will ensure that production operations are carried out in compliance

- Zanesville, OH

Food manufacturing client seeking a Project Engineer for their Zanesville, OH facility. The Project Engineer leads and supports various projects in Capital improvement ranging $5k - $3MM, and operational improvements up to $500k in scope. Must Have:Bachelor’s degree of Engineering required. Preferably in Mechanical Engineering, Chemical Engineering, Process Engineering.5+ years’ experience for projects exceeding $1MM.Comprehensive knowledge of food/beverage engineering principles and....

- Savannah, GA

Food manufacturing client seeking a Project Engineer for their Savannah, GA facility. The Project Engineer leads and supports various projects in Capital improvement ranging $5k - $3MM, and operational improvements up to $500k in scope. Must Have:Bachelor’s degree of Engineering required. Preferably in Mechanical Engineering, Chemical Engineering, Process Engineering.5+ years’ experience for projects exceeding $1MM.Comprehensive knowledge of food/beverage engineering principles and....


POSITION SUMMARY: The Principal Scientist is responsible for method transfer/method verification/co-validation of compendial and non-compendial analytical methods utilized across the company according to written procedures. The testing of routine and non-routine samples where specialized training is essential. Planning and coordination of method transfer/method verification activities in the transfer of analytical methods from the Product Development department or between its facilities.....


Essential Functions: - Knowledge and experience in technologies such as continuous processing, flow chemistry, microwave chemistry is preferred. - Knowledge of and experience with in-situ reaction monitoring technology is preferred. - Knowledge or expertise in principles of operational excellence, six-sigma, and process optimization preferred. - Application of key principles of chemical engineering to work within a matrix-based chemical development team to construct systems and design chemical


Summary We are currently accepting resumes for the position of Research Scientist in Analytical R and D/Methods Development and Validation. ResponsibilitiesMust be fully capable of developing analytical methods based on experience, literature search, etc.Design, develop, conduct and/or review experiments including method development and methodtransfer; perform methods validations utilizing typical instrumentation including but not limited to LC,MS, GC, etc.Interpret data from routine and....


POSITION SUMMARY: Independently responsible for the efficient and thorough investigation of process deviations and customer complaints, determination of root cause, and initiation of corrective/preventative actions designed to adequately address and correct the Quality related deficiencies identified during the investigation process. Responsible to provide proactive corrections based on noted trends to minimize the potential for repeat incidents that may lead to, or result in, the issuance of....


POSITION SUMMARY: My client is seeking an engineer to lead projects in support of small molecule clinical and commercial manufacturing processes. The individual will design, develop, scale-up and optimize robust drug product unit operations that provide high product quality at various scales ranging from R&D to cGMP manufacture. Strong collaboration is expected with internal early R&D groups, internal commercial partners, and external third party CMOs. The candidate should have strong....


My client, a highly regarded New York based research consortium has asked us to search for a Director to lead biologics drug discovery projects in collaboration with academic investigators. You’ll be responsible for lead identification of therapeutic antibodies and proteins, in order to efficiently advance complex research programs from early target validation through animal proof of concept studies. They want a PhD in Immunology, Pharmacology, Molecular or Cell Biology, Biochemistry, or....

- Chicago, IL

$25B Pharmaceutical Company—North Chicago—Salary Commensurate with Experience The SizzleCompany offers great work/life balance.Company offers competitive benefits and perks, including insurance, PTO and sick days, and work flexibility.Company prides itself on having a diverse and inclusive culture. Note from the Hiring ManagerWill provide relocation assistance for the right candidate.Will sponsor an existing H1B. Position Summary Seeking a Senior IT Auditor to be responsible for conducting....


Global Pharmaceutical company is hiring a GLOBAL HEAD RESOURCE MANAGEMENT AND ANALYTICS Position Purpose: Leadership role in Business Operations Management in Clinical Operations with strategic oversight and accountability for the delivery of all aspects of resource planning, capacity management & analytics (metrics) within Clinical Operations.Propose, deliver & implement resource strategies, processes, analyses and tracking for the provision of resource management information to....


Global Pharmaceutical company is looking for a Clinical Partnership Liaison Must have pharmaceutical, Biotech or CRO experience at this senior level. located in NYC must work in the office three days/week The Partnership Liaison is a key leadership role within Clinical Operations Business Operations Management. The role is responsible for implementing and driving the success of the Clinical Development sourcing strategy. The role is accountable for Clinical Development alliances with clinical....


Top Tier Pharmaceutical Company hiring Endocrinologist Field Physician or Senior Field Physician Endocrinology and Diabetes A Field Physician/Sr. Field Physician US Medical Affairs, is a board-certified endocrinologist who has a history of clinical practice, who has significant experience in the therapeutic area of endocrinology and secondary prevention. They will have solid peer relationships with key opinion leaders in their therapeutic area (TA). An ideal candidate should have significant....


Top Tier Pharmaceutical Company hiring Cardiologist Field Physician or Senior Field Physician Cardiology A Field Physician/Sr. Field Physician US Medical Affairs, is a board-certified cardiologist who has a history of clinical practice, who has significant experience in the therapeutic area of cardiology and secondary prevention. They will have solid peer relationships with key opinion leaders in their therapeutic area (TA). An ideal candidate should have significant experience in their....


Director, Medical Information for this leading pharmaceutical company in New England S Headquarters in Waltham, MA Looking for Senior Engineer for drug product unit operations- leadership scale-up and optimization in development from R&D to cGMP Phase 3 manufacture to process validation. Experience with continuous manufacturing, scale-up and PAT implementation is strongly desired. The individual is expected to integrate QbD principles, guide experimental design with a focus on process....


Three Medical Directors needed The Medical Director is a board-certified physician who has a history of clinical practice, and has significant experience in the cardio therapeutic area, Endocrinology or Renal, Nephrology therapeutic areas. The Medical Director is knowledgeable of the actions of regulatory bodies, in particular FDA, and has experience in clinical trials. An ideal candidate should have significant experience in renal cardio disease management and would thrive on proactively....


Pharmaceutical client in NYC hiring two Clinical Research Study Managers for their Global Trials The Clinical Research Study Leader (CRSL) will provide leadership to global Study Management Teams responsible for delivering First in Man, Proof of Concept through to Phase 3 registration studies in various indications. The CRSL will manage a number of studies, either for a single indication or across different indications. The CRSL is accountable for the strategic and tactical study activities,....


The Clinical Operation Lead is responsible for developing operational strategy for one or more clinical studies, and leading the cross-functional Study Management Team to align and deliver on study goals of data quality, timelines, budget and GCP compliance in support of overall program level plans. Responsibilities: The Clinical Operations Lead will independently plan all aspects of the clinical operations for one or more clinical studies and oversee the execution of studies keeping the....

- Albany, NY

Automation Engineer Summary: Responsible for designing, developing, implementing, and maintenance of industrial computerized process control and process monitoring systems in a biopharmaceutical manufacturing cGMP environment. Essential Duties and Responsibilities include, but are not limited to the following: - Provide technical automation support and troubleshooting to Manufacturing, Quality Control, and Facilities according to established SOPs and departmental practices. - Perform....


Principal Automation Engineer Reports to: Automation Manager Summary: Performs advanced technical planning, system integration, maintenance, verification, and validation of PLC and HMI based automated process control systems and process monitoring systems in a biopharmaceutical manufacturing cGMP environment. The Principal Engineer is the site Subject Matter Expert on automated process control and monitoring systems for their area of responsibility and is recognized as a technical expert by....

21-40 of 95 results

Let's get your search started.

Contact Us