Dynamic and goal-oriented professional with extensive knowledge and dedication, seeking a senior production role such as Senior Executive Production, Assistant Manager Production, or Manager Production. Eager to embrace challenging assignments that foster professional development and career growth within a forward-thinking company. Recognized for a pleasing personality and openness to continuous learning and skills enhancement, thriving in diverse and demanding business conditions. Fast learner with exceptional communication skills, driven to motivate teams and achieve organizational and personal goals through hard work and commitment.
Hi, I’m
Sachin Appasaheb Sangale
Production Executive
Boisar,MH
Summary
Overview
19
years of professional experience
1
Certificate
3
Languages
Work History
Aarti Pharma Lab Ltd
Executive Production
08.2018 - Current
Job overview
- Responsible for production of API’s intermediate according to pre-approved instruction.
- Ensure that production facilities are clean and when appropriate, disinfected.
- Distribution of work to optimize manpower supervising of batch charging and verification of RM quantities.
- Monitoring and maintaining of the parameter as per SOP’s.
- Maintaining and updating batch production record online.
- Complying GMP & Safety norms / Independent shift handle.
- Hazop Study / Process trouble shooting, new product batches monitoring.
- Handle all production activities including co-ordination with QA / QC, Store & maintenance Department.
- Ensure the Raw Data Management, Data Integrity and real time documentation are maintained.
- All quality related activities should be recorded in authorized format at the time they performed.
- Any deviation from established procedure should be reported to HOD & QA Department as per laid down SOP.
- Ensuring that all production deviation are reported and evaluated and that critical deviation are investigating and conducting are recorded.
- Execution & Monitoring of Process validation, Cleaning Validation & R&D Batches.
- Identifying the training need for production personnel.
- To actively support the transfer of developed procedures to manufacturing site.
- To contribute to scientific discussions and actively participate in knowledge exchange.
- To optimize planned experimental procedures and reproduce the established ones.
- Monitored & reviewed production, quality, machine and technical efficiencies and reporting.
- Responsible for handling and monitoring the process validation batches as per BPR and protocol and as per current guidelines.
- Monitoring equipment parameters and operational norms with conformance to Standard Operating Procedures (SOP).
- Follow the production planning and accordingly plan activities in shift.
- Responsible for Handling of production documents and review.
- Identify the maintenance problem and get it done.
- Trouble shooting of process/production/ product related problems.
- Regular investigation and analysis of such product/process related issues and having to make necessary contributions to solve them.
- Ensured that all safety and quality measures were adhered to during production process, from beginning to end.
- Expatriation in physical processing like Blending, Milling Packing with customer specification.
- Formerly Known as Aarti Industries Ltd. MIDC- Tarapur- Boisar Maharashtra State.
Emcure Pharma Ltd
Executive Production
03.2017 - 08.2018
Job overview
- Responsible for production of API’s intermediate according to pre-approved instruction.
- Ensure that production facilities are clean and when appropriate, disinfected.
- Distribution of work to optimize manpower supervising of batch charging and verification of RM quantities.
- Monitoring and maintaining of the parameter as per SOP’s.
- Maintaining and updating batch production record online.
- Complying GMP & Safety norms / Independent shift handle.
- Hazop Study / Process trouble shooting, new product batches monitoring.
- Handle all production activities including co-ordination with QA / QC, Store & maintenance Department.
- Ensure the Raw Data Management, Data Integrity and real time documentation are maintained.
- All quality related activities should be recorded in authorized format at the time they performed.
- Any deviation from established procedure should be reported to HOD & QA Department as per laid down SOP.
- Ensuring that all production deviation are reported and evaluated and that critical deviation are investigating and conducting are recorded.
- Execution & Monitoring of Process validation, Cleaning Validation & R&D Batches.
- Identifying the training need for production personnel.
- To actively support the transfer of developed procedures to manufacturing site.
- To contribute to scientific discussions and actively participate in knowledge exchange.
- To optimize planned experimental procedures and reproduce the established ones.
- Monitored & reviewed production, quality, machine and technical efficiencies and reporting.
- Responsible for handling and monitoring the process validation batches as per BPR and protocol and as per current guidelines.
- Monitoring equipment parameters and operational norms with conformance to Standard Operating Procedures (SOP).
- Follow the production planning and accordingly plan activities in shift.
- Responsible for Handling of production documents and review.
- Identify the maintenance problem and get it done.
- Trouble shooting of process/production/ product related problems.
- Regular investigation and analysis of such product/process related issues and having to make necessary contributions to solve them.
- Ensured that all safety and quality measures were adhered to during production process, from beginning to end.
- Expatriation in physical processing like Blending, Milling Packing with customer specification.
Wockhardt Pharma Ltd
Sr. Officer Production
11.2015 - 03.2017
Job overview
- Responsible for production of API’s intermediate according to pre-approved instruction.
- Ensure that production facilities are clean and when appropriate, disinfected.
- Distribution of work to optimize manpower supervising of batch charging and verification of RM quantities.
- Monitoring and maintaining of the parameter as per SOP’s.
- Maintaining and updating batch production record online.
- Complying GMP & Safety norms / Independent shift handle.
- Hazop Study / Process trouble shooting, new product batches monitoring.
- Handle all production activities including co-ordination with QA / QC, Store & maintenance Department.
- Ensure the Raw Data Management, Data Integrity and real time documentation are maintained.
- All quality related activities should be recorded in authorized format at the time they performed.
- Any deviation from established procedure should be reported to HOD & QA Department as per laid down SOP.
- Ensuring that all production deviation are reported and evaluated and that critical deviation are investigating and conducting are recorded.
- Execution & Monitoring of Process validation, Cleaning Validation & R&D Batches.
- Identifying the training need for production personnel.
- To actively support the transfer of developed procedures to manufacturing site.
- To contribute to scientific discussions and actively participate in knowledge exchange.
- To optimize planned experimental procedures and reproduce the established ones.
- Monitored & reviewed production, quality, machine and technical efficiencies and reporting.
- Responsible for handling and monitoring the process validation batches as per BPR and protocol and as per current guidelines.
- Monitoring equipment parameters and operational norms with conformance to Standard Operating Procedures (SOP).
- Follow the production planning and accordingly plan activities in shift.
- Responsible for Handling of production documents and review.
- Identify the maintenance problem and get it done.
- Trouble shooting of process/production/ product related problems.
- Regular investigation and analysis of such product/process related issues and having to make necessary contributions to solve them.
- Ensured that all safety and quality measures were adhered to during production process, from beginning to end.
- Expatriation in physical processing like Blending, Milling Packing with customer specification.
Nectar Life Sciences Ltd
Executive Production
02.2014 - 10.2015
Job overview
- Responsible for production of API’s intermediate according to pre-approved instruction.
- Ensure that production facilities are clean and when appropriate, disinfected.
- Distribution of work to optimize manpower supervising of batch charging and verification of RM quantities.
- Monitoring and maintaining of the parameter as per SOP’s.
- Maintaining and updating batch production record online.
- Complying GMP & Safety norms / Independent shift handle.
- Hazop Study / Process trouble shooting, new product batches monitoring.
- Handle all production activities including co-ordination with QA / QC, Store & maintenance Department.
- Ensure the Raw Data Management, Data Integrity and real time documentation are maintained.
- All quality related activities should be recorded in authorized format at the time they performed.
- Any deviation from established procedure should be reported to HOD & QA Department as per laid down SOP.
- Ensuring that all production deviation are reported and evaluated and that critical deviation are investigating and conducting are recorded.
- Execution & Monitoring of Process validation, Cleaning Validation & R&D Batches.
- Identifying the training need for production personnel.
- To actively support the transfer of developed procedures to manufacturing site.
- To contribute to scientific discussions and actively participate in knowledge exchange.
- To optimize planned experimental procedures and reproduce the established ones.
- Monitored & reviewed production, quality, machine and technical efficiencies and reporting.
- Responsible for handling and monitoring the process validation batches as per BPR and protocol and as per current guidelines.
- Monitoring equipment parameters and operational norms with conformance to Standard Operating Procedures (SOP).
- Follow the production planning and accordingly plan activities in shift.
- Responsible for Handling of production documents and review.
- Identify the maintenance problem and get it done.
- Trouble shooting of process/production/ product related problems.
- Regular investigation and analysis of such product/process related issues and having to make necessary contributions to solve them.
- Ensured that all safety and quality measures were adhered to during production process, from beginning to end.
- Expatriation in physical processing like Blending, Milling Packing with customer specification.
Orchid Chemicals & Pharmaceuticals Ltd
Officer Production
05.2007 - 01.2014
Job overview
- Responsible for production of API’s intermediate according to pre-approved instruction.
- Ensure that production facilities are clean and when appropriate, disinfected.
- Distribution of work to optimize manpower supervising of batch charging and verification of RM quantities.
- Monitoring and maintaining of the parameter as per SOP’s.
- Maintaining and updating batch production record online.
- Complying GMP & Safety norms / Independent shift handle.
- Hazop Study / Process trouble shooting, new product batches monitoring.
- Handle all production activities including co-ordination with QA / QC, Store & maintenance Department.
- Ensure the Raw Data Management, Data Integrity and real time documentation are maintained.
- All quality related activities should be recorded in authorized format at the time they performed.
- Any deviation from established procedure should be reported to HOD & QA Department as per laid down SOP.
- Ensuring that all production deviation are reported and evaluated and that critical deviation are investigating and conducting are recorded.
- Execution & Monitoring of Process validation, Cleaning Validation & R&D Batches.
- Identifying the training need for production personnel.
- To actively support the transfer of developed procedures to manufacturing site.
- To contribute to scientific discussions and actively participate in knowledge exchange.
- To optimize planned experimental procedures and reproduce the established ones.
- Monitored & reviewed production, quality, machine and technical efficiencies and reporting.
- Responsible for handling and monitoring the process validation batches as per BPR and protocol and as per current guidelines.
- Monitoring equipment parameters and operational norms with conformance to Standard Operating Procedures (SOP).
- Follow the production planning and accordingly plan activities in shift.
- Responsible for Handling of production documents and review.
- Identify the maintenance problem and get it done.
- Trouble shooting of process/production/ product related problems.
- Regular investigation and analysis of such product/process related issues and having to make necessary contributions to solve them.
- Ensured that all safety and quality measures were adhered to during production process, from beginning to end.
- Expatriation in physical processing like Blending, Milling Packing with customer specification.
Sun Pharma Ltd
Production EPP Trainee
10.2006 - 03.2007
Job overview
- Responsible for production of API’s intermediate according to pre-approved instruction.
- Ensure that production facilities are clean and when appropriate, disinfected.
- Distribution of work to optimize manpower supervising of batch charging and verification of RM quantities.
- Monitoring and maintaining of the parameter as per SOP’s.
- Maintaining and updating batch production record online.
- Complying GMP & Safety norms / Independent shift handle.
- Hazop Study / Process trouble shooting, new product batches monitoring.
- Handle all production activities including co-ordination with QA / QC, Store & maintenance Department.
- Ensure the Raw Data Management, Data Integrity and real time documentation are maintained.
- All quality related activities should be recorded in authorized format at the time they performed.
- Any deviation from established procedure should be reported to HOD & QA Department as per laid down SOP.
- Ensuring that all production deviation are reported and evaluated and that critical deviation are investigating and conducting are recorded.
- Execution & Monitoring of Process validation, Cleaning Validation & R&D Batches.
- Identifying the training need for production personnel.
- To actively support the transfer of developed procedures to manufacturing site.
- To contribute to scientific discussions and actively participate in knowledge exchange.
- To optimize planned experimental procedures and reproduce the established ones.
- Monitored & reviewed production, quality, machine and technical efficiencies and reporting.
- Responsible for handling and monitoring the process validation batches as per BPR and protocol and as per current guidelines.
- Monitoring equipment parameters and operational norms with conformance to Standard Operating Procedures (SOP).
- Follow the production planning and accordingly plan activities in shift.
- Responsible for Handling of production documents and review.
- Identify the maintenance problem and get it done.
- Trouble shooting of process/production/ product related problems.
- Regular investigation and analysis of such product/process related issues and having to make necessary contributions to solve them.
- Ensured that all safety and quality measures were adhered to during production process, from beginning to end.
- Expatriation in physical processing like Blending, Milling Packing with customer specification.
Education
Pune Board
S.S.C
01.2001
University Overview
GPA: 73.33%
Vinayaka Mission UniversityTamil Nadu
M.SC from General Chemistry
01.2016
University Overview
GPA: 63.00%
MSBTEMumbai
Advance Diploma in Industrial Safety
01.2012
University Overview
GPA: 63.00%
Pune University
B.SC from Chemistry
01.2006
University Overview
GPA: 66.00%
Pune Board
H.S.C
01.2003
University Overview
GPA: 53.67%
Skills
Judgment and decision making
Interests
Playing Badminton
Traveling with friends
Wandering in nature
Personal Information
Personal Information
- Height: 5.4
- Passport Number: X3436021
- Passport Expiry Date: 2029-12-31
- Father's Name: Appasaheb Dadaba Sangale
- Number of Children: 2
- ID Type: Passport
- ID Number: X3436021
- Date of Birth: 27/11/1985
- Gender: Male
- Nationality: Indian
- Marital Status: Married
Addresses
Addresses
Current Address - Flat No. 401, 4th Floor, F-Wing, Balaji Realtors, Building No. 18, Yashwant Shrusti, Palghar Boisar Road, Boisar, Maharashtra, 401501,
Permanent Address - H. No. 01, Near Ganpati Temple, At: - Chitali, Post: - Padali, Pathardi, Maharashtra, 414505
Salary Expectation
Salary Expectation
As per company policyJoining Period
Joining Period
Sixty Days after receiving job offer letterPersonal data processing
Personal data processing
I hereby declare that all the statement made by me is true and complete to the best of my knowledge and belief and nothing has been suppressed.Certification
SAP PP module
Reading Books , Playing Cricket
Reading Books , Playing Cricket
Im Sachin Sangale working as Pharmacist, actively reading books and playing cricket and listening song .
Timeline
SAP PP module
08-2025
Executive Production
Aarti Pharma Lab Ltd
08.2018 - Current
Executive Production
Emcure Pharma Ltd
03.2017 - 08.2018
Sr. Officer Production
Wockhardt Pharma Ltd
11.2015 - 03.2017
Executive Production
Nectar Life Sciences Ltd
02.2014 - 10.2015
Officer Production
Orchid Chemicals & Pharmaceuticals Ltd
05.2007 - 01.2014
Production EPP Trainee
Sun Pharma Ltd
10.2006 - 03.2007
Vinayaka Mission University
M.SC from General Chemistry
MSBTE
Advance Diploma in Industrial Safety
Pune University
B.SC from Chemistry
Pune Board
H.S.C
Pune Board
S.S.C