MEDVACON Life Sciences is open to meeting a Director of Operations for a perm role based in Sparta NJ.  The role is on-site for local employees and can be remote/partial remote for candidates outside of the local area.

Provide tactical, strategic and operational leadership for the successful delivery of consulting engagements including:

·         Project Management

·         Client Relationship Building

·         Business Development

·         Strategic Planning

Accountabilities:

1.       Provide oversight and management of consultants in addition to projects / work. Manage work (physical project completion and outcome) and also manage people. 

2.       Provide trusted advisory and technical/regulatory SME to client stake-holders gaining trust and buy-in with MLS

3.       Provide expert project manager services bringing client engagements to successful completion on time and within budget.

4.       Create and execute strategies with client teams

5.       Serve as billable Consultant and/or lead resources on certain client projects

6.       Track project progress and status

7.       Participate in regular leadership meetings providing project status reports, successes and potential issues

8.       Identify opportunities for additional work on client projects.

9.       Conduct technical review and revision of client Standard Operating Procedures

10.   Create proposals

11.   Participate on client BD calls as SME

12.   Build and maintain long-term client relationships resulting in repeat business and client reference

13.   Develop successful project teams and participate in the candidate interview and selection process.

14.   Direct technical managers, delivery consultants and industry specialists

1.       Bachelor’s degree in Life Sciences, advanced degree preferred

2.       PMI preferred

3.       10+ ys Managing Life Sciences Quality and Compliance consulting services

4.       Prior hands on exp in an FDA regulated setting in the following areas Desired:

·         Equipment, Facility and Utility Qualification

·         Computer system Validation

·         Cleaning Validation

·         Process Validation

·         Quality System Assessments and Implementation

·         Auditing and Gap cGMP Gap Assessments

·         Manufacturing Operations in Pharma, Bio-Pharma and/or Medical Device

·         Process Engineering

5. Open to occassional travel

NO! Agencies or 3rd party agencies.  We do not work through other employers

NO WORK PERMITS

Please attach a WORD resume to your submission

All of your information will be kept confidential according to EEO guidelines.

EOE/Veteran/Disabled