USA Ramsey
In the overview below you will find the job vacancies available at this location. If any of the offers match your profile, please click on the corresponding position for a detailed description.
We are not accepting candidates submitted through recruiters for any position listed.
Automation Engineer (I)
The ability to develop (not modify), test, and commission Allen Bradley PLC (ControlLogix and/or PLC-5) control system applications using RSLogix. Higher level skills that are desirable include analog data handling, data exchanges, batch sequencing (S88), recipe handling, etc.
The ability to develop (not modify), test, and commission SCADA (iFix and/or Wonderware) control system applications. Higher level skills that are desirable include scripting, security configuration, recipe configuration, database interfacing, report configuration, etc.
Business Development Manager - Pharmaceutical Services
Identify and close new pharmaceutical solid dosage product development and manufacturing projects and opportunities. Build and maintain relationships and assure customer satisfaction with key accounts. Participate in the development and implementation of pharmaceutical advertising, marketing and sales strategies. Participate in applicable pharmaceutical industry associations, including attendance and public speaking engagements at shows, seminars, conferences, etc. 10-15% overnight travel.
Chemist
Masters required in Chemistry plus 6 months of experience. Test raw materials, in process, prototype formulation drug products, finished products submitted and/or produced by the formulation/development lab and contract manufacturing. Experience in dissolution apparatus, Nicolet Avatar 370 Infrared Spectrometer, Malvern Laser based particle size analyzer, and gas chromatograph. Apply with 2 copies of resume to HR, Glatt Air Techniques, Inc., 20 Spear Road, Ramsey, NJ 07446 Attn: D. Lancaster
Director, Compliance and Quality Assurance
Candidates must have a degree in Chemistry, Pharmacy or related discipline with a minimum of 10 years experience in Quality Assurance and some analytical laboratory experience. Candidates must also have at least 2 years of management or supervisory experience. Candidates must have a thorough knowledge of pharmaceutical GMPs and contemporary Validation requirements. Candidates who also have past pharmaceutical manufacturing experience are preferred. Candidates must have prior experience in dealing with the FDA and other regulatory agencies. Candidates must be detail‑oriented with excellent written and oral communication skills. Candidates must be capable of creating and working within a budget. Computer literacy is also required.
Director of Process Optimization and Technical Staff Development
The primary responsibility of the candidate is to provide support in the technical area of GAT’s manufacturing processes. This will include acting as the technical liaison between Sales and our clients. This role will act as the czar for all operational training as it relates to pharmaceutical processing.
Project Engineer
Overnight travel up to 60% (80% including local travel) or as needed to complete responsibilities. Fulfill technical and field start-up responsibilities for all projects assigned by department supervisor. These include but are not limited to: technical sales support, design and ordering of support systems, review of system documents and drawings (mechanical, controls and validation), customer assistance, start-up of machine systems, training of machine users, preventive maintenance equipment reviews, rebuilds, site engineering evaluations and controls service.
Bachelor of Science in Engineering, or Computer Science. Experience with psychometrics, hydraulics, pneumatics, variable frequency drives, Allen Bradley PLC ladder logic and basic welding and metalworking. Familiarity with industry standards such as NFPA, NEC, and NEMA.
Project Manager
Prepare equipment and service quotations including man hour estimates and purchased item costs for all GAT products and services. Process equipment orders, develop and maintain project schedules, monitor project budgets and review/approve all order design documents for manufacturing. Source, engineer and evaluate capital equipment for use in GAT system quotes. Act as main customer-project liaison. Travel up to 10% to customer sites to perform project coordination.
BS/BE in Engineering. 5 to 10 years project management or related experience. Candidate must have pharmaceutical industry and experience in specifying and purchasing pharmaceutical manufacturing capital equipment.
QA Technician (3:30pm to midnight)
Interaction with customers on quality issues. Issue batch records and labels for GMP batches. Review documents for accuracy, process compliance and completion. Inspect for and promote cGMP compliance in the processing suites and warehouse. Ability to maintain documents neatly and accurately. Must be able to lift and handle up to and including 25 kg weights, as required. Alternate shift/hours and weekends are required as scheduled
Experience in the pharmaceutical industry. Bachelor’s Degree in Science field desired.)