Executive Recruiter,
Medical Devices and Engineering
Mr. Lindsay Allen

Your resume is held in strict confidence, all fees are employer paid, and relocation assistance is provided for all qualified persons unless otherwise stated.

We are currently seeking candidates for the job opportunities as listed below.
Please contact Mr. Lindsay Allen for details
Send your resume to:  lallen@spassociates.com
Toll Free:  866-488-6677 or Local:  704-643-7250
Fax:  704-643-1249

Updated January 2007

Opportunities

SENIOR PROJECT ENGINEER Job Summary: Responsible for the reliability and continuous improvement of the automated equipment in pharmaceutical manufacturing. Job Details: Establish baseline equipment capabilities and work to improve those capabilities. Identify constraints in the automated manufacturing flow and eliminate or improve those constraints to achieve a balanced process flow. Identify and minimize factors that contribute to manufacturing defects. Support the manufacturing mechanics with advanced troubleshooting. Work with the manufacturing supervisors to implement identified process improvements. Work to ensure that the company is in compliance with all environmental, health and safety requirements and assure our business practices enhance the welfare of our customers, employees, and the community in which we operate. This position has full responsibility and authority to make necessary decisions and/or take action that is required to carry out job duties. Incumbent will follow all Safety, 5S housekeeping, and cGMP procedures. Education and Experience: B.S. in Engineering and at least eight (8) years of experience with at least four (4) years of experience in the pharmaceutical industry. Must have a comprehensive engineering knowledge and a broad business knowledge. Salary: $85-105K Location: Texas

COMPOUNDING SUPERVISOR Job Summary: Supervises the daily operations of a manufacturing area in a pharmaceutical plant. Job Details: Includes ensuring all necessary components/resources are available and capable to meet production schedule and established quality standards and goals; that all department operations are in compliance with cGMP/ISO regulations, as well as meeting production standards. Directly responsible for supervising the daily activities of employees by providing training, direction, guidance, counseling or disciplinary action when necessary, and, in conjunction with HR, makes decisions regarding personnel actions (hiring, terminations, promotions, etc.). Services as mentor to supervisory staff through training and leadership. Responsible for success of one or more areas and shifts. This is a regulated company and the incumbent is expected to be fully compliant with all criteria established by governmental agencies, Boards of Health, and legislative requirements including, but not limited to: the FDA, EMEA, ISO 13485:2003/CMDCAS, Canadian Medical Device Regulations (CMDR), OSHA, Sarbanes-Oxley, EPA, EEOC, and ADA. Incumbent has full authority to make decisions and/or take action that is required to carry out job duties. Follows all Safety, 5S housekeeping, cGMP procedures, and must be willing to take temporary assignments as required. Jobs Supervised: Hourly employees in assigned work areas. Education and Experience: BS or BA in Business or Technical Field required. Minimum four (4) years experience in supervision. Broad understanding of management and technical details of the manufacturing processes, including cGMP/QSR. Demonstrated managerial ability. Salary: $55-70K Location: Texas

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We have many other opportunities that are not listed above.  Please contact us and let us know what job opportunities you are seeking.