Manufacturing Engineer

Job Title: Manufacturing Validation EngineerFLSA Classification: Professional, ExemptWork Location: Fall River, MAWork Hours: General Shift: 8:30AM – 5:00PM (may vary based on business needs)Reports To: Manufacturing ManagerJob DescriptionThe Manufacturing Validation Engineer is responsible for the creation and revision of new and existing GMP, project handle, qualification & validation documents preparation and execution. In this role the Validation Engineer adheres to the company's document and SOP's procedures while ensuring their accuracy, quality, and integrity. This position reports to the Manufacturing/Packaging and partners with cross functional team members to ensure compliance and operational success through user focused documentation.The job duties for this position include but are not limited to the following:Develop appropriate disposition metrics, works with manufacturing/packaging personnel to achieve said targets. Generates and reports on metrics on an agreed frequencyCreates training materials for subject matter input.Track and manage periodic review.Develop strategies and documents for cleaning and process validation of API equipment and products in compliance with site SOPs and regulatory guidance.Autonomously leads and manages projects to implement continuous improvement opportunities.Lead and/or support root cause investigations related to performance trends and formal deviations.Develop, implement and assess solutions for complex problems. Anticipates risk and builds contingencies to help mitigate impact.Reviews documents for accuracy and completeness.Defends the validation programs and strategies to customers and regulatory auditors.Performs weekly quality reviews of Master Control database by assuring new documents have been entered using appropriate protocols.Follows strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Manufacturing Practices (cGMP), complying with legal regulations, monitoring environment.Performs other duties as assigned.Knowledge of qualification and validation documents.Preparation of qualification and validation documents of equipment and computer system.Preparation and qualification of e-batch record & e-Log Book.Knowledge of cleaning validation and process validation.Knowledge in project handle with new equipment.Knowledge of URS, FDS, DQ, HDS, SDS, FS, validation plan, FAT, SAT, IQ, OQ, PQ, validation certificate, PIR, RTM, electronic signature, electronic reports.Knowledge of 21 CFR and implementation. Knowledge of automation of pharmaceutical equipment.Education and ExperienceAssociate's degree with 4-6 years knowledge and experience of GMP documentation required.Bachelor's degree in science, biochemistry, pharmaceutical engineering, Pharmaceutical Sciences, or related discipline from an accredited college/university (preferred).Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study from an accredited college/university preferred.Minimum four (4) years documentation experience and six (6) years related pharmaceutical or biotech industry experience. Preference will be given to candidates with experience in generic pharmaceutical manufacturing.Technical Knowledge and Computer Systems SkillsExcellent communication skills, drive, and sense of urgencyExcellent computer skills, specifically Microsoft Office Suite.Solid organizational and time management skills are required to prioritize activities in a manner consistent with departmental and site wide objectives.Follow strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Manufacturing Practices (cGMP), complying with legal regulations, monitoring environment.Must have ability to work as a self-starter and handle multiple priorities in a dynamic cross-functional team-based environment.Knowledge of pharmaceutical manufacturing and related documents.Knowledge and experience writing, revising and creating cGMP records and SOPs.Knowledge of GDP.Creation and maintenance of batch record and cGMP documentation templates.Hands‑on experience facilitating problem solving and root cause investigations in a pharmaceutical environment - Develops, implements, and assesses solutions for complex problems.Ability to work effectively both independently and as part of a team.Capable of handling and participating in compliance and regulatory audits at the local and federal levels.Experience using SAP business system and applications is a plus.Experience in Inhalation products (MDI) is a plus.Knowledge and handling of deviation, CAPA, change control, FMECA and training.Knowledge and handling of SAP system, master control and track wise system.During audit part of team.Knowledge of audits and compliance.Professional and Behavioral CompetenciesProficiently speak English as a first or second languageAbility to understand and analyze complex data sets.Knowledge of statistical packages is a plus.Knowledge of good manufacturing practices and good documentation practices preferred.Ability to read, write and communicate effectively.Self‑motivated, with the ability to work in a fast‑paced manufacturing environment and handle multiple tasks simultaneously.Position requires flexibility to quickly adapt to changing work environment and schedulesExcellent organizational skills with the ability to focus on details.Basic computer skills (Word and Excel) – IntermediateGood basic math knowledge and excellent attention to details.Work Schedule and Other Position InformationMust be willing to work in a pharmaceutical manufacturing setting.Must be willing to work some weekends based on business needs as required by management.No remote work available.Seniority levelMid‑Senior levelEmployment typeFull‑timeJob functionProduction, Manufacturing, and OtherIndustriesPharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment ManufacturingBenefitsMedical insurance, Vision insurance, 401(k)#J-18808-Ljbffr