CAREERS
At Halo Pharma, we believe it is our people that make us a different kind of partner. We are comprised of experienced professionals who are committed to innovation, excellence, and customer service. We welcome new colleagues who are interested in being part of our dynamic team and who are inspired to build partnerships that make a difference. Thank you for your interest in Halo Pharma.
CURRENT OPENINGS
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Senior Validation Specialist Job Description
Duties and Responsibilities:
Conducts qualification and validation studies for manufacturing processes, equipment, utilities and cleaning validation.
Provides technical assistance, as needed, for manufacturing and engineering troubleshooting.
Responsible for the coordination of supportive validation activities (such as laboratory testing, calibration, scale-up and engineering studies) and assurance that the necessary project documentation is complete, accurate and in compliance with cGMP regulations.
Evaluate qualification and validation projects to establish technically and scientifically sound protocols and test plans.
Execute protocols by carrying out the preapproved testing in the operations and laboratory areas.
Collect and analyze all data, write final report and obtain approvals.
Review technical documentation (batch records, SOPs, calibration records, preventive maintenance work orders, protocols, reports) for continuity and accuracy.
Perform gap assessments and remediation as required on legacy qualification and validation packages.
Write SOPs and protocols to support departmental programs and projects.
Evaluate, maintain and operate validation instrumentation as required in order to support assigned projects (examples: Kaye Validator 2000, dew point monitor).
Coordinate successful execution of projects by working effectively with cross-functional groups.
May interface with the FDA and customers during site audits to respond to validation-related questions.
May be involved in investigation and root cause analysis for incidents reported on validated systems.
Requirements:
Bachelor’s degree in Engineering, or in a scientific discipline, or equivalent experience.
At least 6 years of demonstrated direct (hands-on) validation experience in at least three of the following areas: tablet manufacturing/finishing, equipment. qualification, sterile/aseptic operations, finishing operations, utilities qualification, active ingredient synthesis, automated controller/computer qualification, cleaning validation.
Ability to work harmoniously and effectively with others in a fast-paced environment.
Ability to effectively communicate technical information in a clear, concise English language (written and verbal) within a GMP - regulated environment.
Flexibility to work off-hours and weekends as required to support manufacturing plant projects.
Ability to effectively manage multiple projects simultaneously (3-6 typical).
To apply, please submit your resume to
HumanResources@halopharma.com 
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Temporary – Pharmaceutical Packaging Operator
Duties and Responsibilities:
Set up and operates a packaging machine in accordance with established procedures and guidelines. Fill, secure, and label containers according to company and/or customer specifications. Verify goods packaged against package invoices. Reports to the Packaging Supervisor and receives daily direction from the Packaging Group Lead. May have the potential to become a regular, non-temporary, position.
Requirements:
Pharmaceutical Packaging experience is required as well as knowledge of commonly used concepts, practices, and procedures within the Pharmaceutical Industry. Be able to understand and follow spoken and written instructions and pre-established guidelines and SOPs to perform the functions of the job. Must be able to work overtime as requested.
To apply, please submit your resume and salary expectations to
HumanResources@halopharma.com
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