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We are looking for a Quality Control Analyst who will support the Quality Control group to maintain process optimization and manufacturing activities. This person will be reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in the QC lab with....


We are looking for a Technical Services Scientist who will be responsible for working on all aspects of the technology transfer for sterile drug products, specifically Lyophilized and vial products, pre-filled syringes, and Blow-Fill-Seal (BFS) products. This would include working with Formulation and Analytical Development, Quality, Production and Regulatory to identify product and process criticalities and how to maintain them along with finding creative solutions to any roadblocks in the....


We are looking for a Calibration / Instrument / Metrology Technician who will initiate, coordinate, and administer the calibration program for the facility. They will conduct/coordinate the inspection, calibration, and repair of all instruments, equipment and systems used for the manufacturing and measurement and determination of quality attributes of pharmaceutical products in accordance with current industry regulations and practices in the U.S.A. and the state of North Carolina.Under the....


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


If you are an experienced Food Safety Manager in the prepared/packaged food industry and are looking for an opportunity to make an impact, this may be the place for you! Top 5 Requirements: 1. Bachelor’s degree in Food Science, Microbiology, Biology or related field is Required.2. Product experience should include food products.3. Technical knowledge of food safety, food science, and regulatory requirements is a must.4. Ability to demonstrate an understanding of process control methods and....

- Shorewood Hills, WI

This full time, permanent Mechanical Engineer opportunity is at a smaller company that prides itself on being innovative. Their products deal with integrating imaging in industry. The company is growing and they recently set a revenue record. The successful candidate will be a part of the design layout, product specification execution and system builds. There is a lot of autonomy with this position but you will also work with a great group of talented individuals. This position could grow into


Here is an excellent growth opportunity with a prominent food products manufacturer! Plant Sanitation Manager -- Cleveland, OH -- 6 day week (6 days, 10 hours per day) -- $78-85,000 -- Excellent benefits -- Relocation Assistance Responsibilities of the Sanitation Manager: - Manages the company's sanitation department. to requirements for food processing machinery, equipment, and facility - Includes assisting in planning, scheduling, assigning and directing of sanitation personnel (approx:....


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....


KEY AREAS OF JOB ACCOUNTABILITY: (list of key objectives and quantifying standards) The holder of this position is charged with leading effort to prove control of the critical aspects of company operations, whether these relate to process, cleaning, equipment, utilities, computers or other elements. Specific emphasis will be placed on Process and Cleaning Validation.Subject matter expert in at least two main area of validation ( Process/Cleaning/Equipment /Utilities /Facilities/Computer....


My client seeks a Computational Chemist Post Doc to study molecules and prepare safety assessments on materials and natural complex substances. The ideal candidate will take on the following tasks:Use modeling and in-silico sources to derive data to support risk assessments for molecules.Work closely with a group of toxicologists, safety assessors, and other scientists to ensure molecule safety.Identify clusters and scientifically valid read across materials to complete endpoint....


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....

- Jersey City, NJ

Pharmaceutical company in Jersey City, NJ in need of Clinical Research Associate Responsible for monitoring of single and multi-site clinical trials. Assures adherence to international Commission on Harmonization (ICH), Good Clinical Practices (GCP), and Code of Federal Regulations (CFR). Assures compliance with institutional Standard Operating Procedures (SOPs) and Policies, protocol requirements, and institutional reporting requirements. Performance of this position requires coordination and

- Any US State

Global Pharmaceutical company is hiring Clinical Project Manager for their Clinical Development studies Day to day management of studies This position is responsible for providing oversight of Phase 1 to Phase 4 clinical trial implementation; ensuring clinical studies are conducted in a timely manner with milestones being achieved within budget.Essential FunctionsThe Clinical Project Manager for this Pharmaceutical company- will:Utilize Project Management techniques and methodologies to plan,....


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 hiring three Clinical Operations Directors (Vaccine or rare disease or Oncology) This position will be responsible for initiating and leading phase 1 and 2 clinical trials development, set-up, implementation and completion. This will be accomplished by working with the internal project team and through a preferred provider CRO and other external contractors. This role will report internally to the Head of Clinical Operations and work closely with the Regulatory


Top Tier Pharmaceutical company (with focus in RESPIRATORY, CNS, Diabetes, Cardio, GI and more) in Madison, NJ is looking for three Clinical Trials Manager Consultants for Clinical Trials Group This is a one year contract and can continue for up to 4 years (1099 or w-2)SummaryParticipate in all aspects of clinical development and study management under the direction of the Director, or designee, which includes providing scientific, and/or logistical support to planned and ongoing trials CTM –....


The Senior Manager, Clinical Development CNS will participate in internal process improvement activities within R&D and Clinical Development. Main Areas of Responsibilities supports the Clinical Program Lead and Clin.Sci. Lead in the development of the Clinical Development Plan and associated clinical trial content (e.g., protocols, IBs/IDFUs, CRFs, CSRs, regulatory submissions and publications) by contributing to scientific/clinical information aligned with the strategy. key Clinical....

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