Cipla USA
Job Title
Pkg. Documentation Specialist II
FLSA Classification
Professional, Exempt
Work Location
Fall River, MA
Work Hours
General Shift: 8:30AM - 5:00PM (may vary based on business needs)
Reports To
Department Head - Manufacturing
Salary Range
$72,800 - $93,600
Job Overview Invagen Pharmaceuticals is searching for experienced candidates for the position of Documentation Specialist. The Documentation Specialist is responsible for the creation and revision of new and existing GMP batch production records as well as SOPs. In this role the Documentation Specialist adheres to the company\'s document and SOP procedures while ensuring their accuracy, quality, and integrity. This position reports to the Department Head - Manufacturing and partners with cross functional team members to ensure compliance and operational success through user focused documentation at InvaGen Pharmaceuticals, Inc, Fall River, MA.
Responsibilities
Works with Manufacturing/Packaging to deliver timely batch record review across all shifts.
Reviews and approval of master batch records.
Develops appropriate disposition metrics, works with manufacturing/packaging personnel to achieve said targets. Generates and reports on metrics on agreed frequency
Creates training materials for subject matter input.
Track and manage periodic review of approved procedures.
Develop strategies and documents for cleaning and process validation of equipment and products in compliance with site SOPs and regulatory guidance.
Provides data to support management evaluation of performance trends.
Owns quality records (change control, CAPAs, deviations) and delivers to established timelines.
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 document 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 the environment.
Performs other duties as assigned.
Education and Experience
Associate 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.
Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study from an accredited college/university preferred.
Minimum two (2) years documentation experience and four (4) years related pharmaceutical or biotech industry experience. Preference will be given to candidates with experience in generic pharmaceutical manufacturing.
Technical Knowledge and Computer Systems Skills
Excellent communication skills, drive, and sense of urgency
Excellent 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 the environment
Must have ability to work as 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
Closure of any compliance related CAPAs
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, OOS, OOT, training and OOAC
Knowledge and handling of SAP system, master control and TrackWwise system
Knowledge of preparation of BMR and eBMR
Knowledge of preparation of SOP and eLog books
During audit part of team
Planning of batches as per production plan
Knowledge of audits and compliance
Professional and Behavioral Competencies
Proficiently speak English as a first or second language
Ability 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 schedules
Excellent organizational skills with the ability to focus on details
Basic computer skills (Word and Excel) - Intermediate
Good basic math knowledge and excellent attention to details
Work Schedule and Other Position Information
Must be willing to work in a pharmaceutical manufacturing setting
Must be willing to work some weekends based on business needs as required by management
Relocation negotiable
No remote work available
Global Company Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India\'s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla\'s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.
CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.
Cipla, Inc is an equal opportunity and affirmative action employer committed to building an inclusive and diverse workforce.
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Pkg. Documentation Specialist II
FLSA Classification
Professional, Exempt
Work Location
Fall River, MA
Work Hours
General Shift: 8:30AM - 5:00PM (may vary based on business needs)
Reports To
Department Head - Manufacturing
Salary Range
$72,800 - $93,600
Job Overview Invagen Pharmaceuticals is searching for experienced candidates for the position of Documentation Specialist. The Documentation Specialist is responsible for the creation and revision of new and existing GMP batch production records as well as SOPs. In this role the Documentation Specialist adheres to the company\'s document and SOP procedures while ensuring their accuracy, quality, and integrity. This position reports to the Department Head - Manufacturing and partners with cross functional team members to ensure compliance and operational success through user focused documentation at InvaGen Pharmaceuticals, Inc, Fall River, MA.
Responsibilities
Works with Manufacturing/Packaging to deliver timely batch record review across all shifts.
Reviews and approval of master batch records.
Develops appropriate disposition metrics, works with manufacturing/packaging personnel to achieve said targets. Generates and reports on metrics on agreed frequency
Creates training materials for subject matter input.
Track and manage periodic review of approved procedures.
Develop strategies and documents for cleaning and process validation of equipment and products in compliance with site SOPs and regulatory guidance.
Provides data to support management evaluation of performance trends.
Owns quality records (change control, CAPAs, deviations) and delivers to established timelines.
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 document 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 the environment.
Performs other duties as assigned.
Education and Experience
Associate 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.
Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study from an accredited college/university preferred.
Minimum two (2) years documentation experience and four (4) years related pharmaceutical or biotech industry experience. Preference will be given to candidates with experience in generic pharmaceutical manufacturing.
Technical Knowledge and Computer Systems Skills
Excellent communication skills, drive, and sense of urgency
Excellent 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 the environment
Must have ability to work as 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
Closure of any compliance related CAPAs
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, OOS, OOT, training and OOAC
Knowledge and handling of SAP system, master control and TrackWwise system
Knowledge of preparation of BMR and eBMR
Knowledge of preparation of SOP and eLog books
During audit part of team
Planning of batches as per production plan
Knowledge of audits and compliance
Professional and Behavioral Competencies
Proficiently speak English as a first or second language
Ability 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 schedules
Excellent organizational skills with the ability to focus on details
Basic computer skills (Word and Excel) - Intermediate
Good basic math knowledge and excellent attention to details
Work Schedule and Other Position Information
Must be willing to work in a pharmaceutical manufacturing setting
Must be willing to work some weekends based on business needs as required by management
Relocation negotiable
No remote work available
Global Company Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India\'s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla\'s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.
CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.
Cipla, Inc is an equal opportunity and affirmative action employer committed to building an inclusive and diverse workforce.
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