Senior Quality Engineer
Synectics
Description :
- The Senior Quality Engineer is responsible for carrying out Manufacturing Quality Assurance functions within the plant.
- The Senior Quality Engineer will provide Quality support for projects related to core production, new software/computer systems, new products/technologies/Automation systems.
- As part of the project team, the Senior Quality Engineer will ensure all activities including Qualification/Validation Strategy, Deviation Investigation and Resolution, Risk Management activities, etc. meet applicable Quality and Regulatory requirements.
- Additionally, the Senior Quality Engineer supports on-going production including by working with operations/quality teams for deviation resolution, auditing of commissioning and validation documentation completed by others, authoring and execution of newly identified qualification/validation protocols, review and approval of critical planned maintenance routines, and other quality assurance tasks assigned by the MQA Section Manager and/or the Plant QA Manager.
- Responsible for implementing and maintaining the effectiveness of the Quality System.
- Support the site to ensure that all quality goals are met, and all practices and procedures comply with company policies and applicable regulations for the Quality areas under his/her responsibility.
- Provide Quality support on project work related to Equipment installation/Computer Systems/Automation Systems while ensuring compliance with applicable regulations/standards.
- Lead project activities related to Quality and Compliance.
- Support Core production/ process improvement projects as assigned.
- Oversee data integrity initiatives to ensure security, accuracy, consistency, and completeness of data throughout system usage.
- Support the Risk Management process throughout all quality system elements such as Design Control, Product Surveillance, Field Action, etc.
- Update risk management file documents as needed.
- Ensures investigations of plant events are completed thoroughly and documented accurately and are included in the plant CAPA system.
- Performs product impact analyses for plant events and places product on QA hold where appropriate.
- Maintains an effective liaison and cooperative relationship with other Quality areas and Plant departments including remote off-shift support as required.
- Approves standard operating procedures; ensures procedures comply with policies and regulations.
- Bachelor's degree, preferably in Biology, Chemistry or Engineering
- 6+ years of overall experience in Manufacturing, Quality or Engineering
- Good verbal and written communication skills.
- Good problem solving and analytical skills
- Good interpersonal relations / communications skills
- Good negotiation skills
- Knowledge of quality / compliance management as well as regulations and standards affecting API, Bulk Drug or Finished goods manufacturing.
- Experience in manufacturing within pharmaceutical, medical device, biotechnology and food industry with cGMP is highly desirable
- Experience with implementing and maintaining the effectiveness of the Quality System.
- Quality System and Regulatory Knowledge - Strong knowledge of ISO 13485, !SO 14971 and FDA 21 CFR part 820/QSMR
- Risk management and FMEA understanding
- Technical problem Solving and Root cause analysis expertise
- Communication and Cross-Functional Influence
- Manufacturing Quality Experience and process knowledge
- Shift time:M-F 8 am - 5 pm; Rotating weekly on-call shifts for evenings and weekends
Vacancy posted 1 day ago
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